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1.
Eur J Hum Genet ; 31(7): 824-833, 2023 07.
Article in English | MEDLINE | ID: mdl-37130971

ABSTRACT

Amino-terminal (Nt-) acetylation (NTA) is a common protein modification, affecting 80% of cytosolic proteins in humans. The human essential gene, NAA10, encodes for the enzyme NAA10, which is the catalytic subunit in the N-terminal acetyltransferase A (NatA) complex, also including the accessory protein, NAA15. The full spectrum of human genetic variation in this pathway is currently unknown. Here we reveal the genetic landscape of variation in NAA10 and NAA15 in humans. Through a genotype-first approach, one clinician interviewed the parents of 56 individuals with NAA10 variants and 19 individuals with NAA15 variants, which were added to all known cases (N = 106 for NAA10 and N = 66 for NAA15). Although there is clinical overlap between the two syndromes, functional assessment demonstrates that the overall level of functioning for the probands with NAA10 variants is significantly lower than the probands with NAA15 variants. The phenotypic spectrum includes variable levels of intellectual disability, delayed milestones, autism spectrum disorder, craniofacial dysmorphology, cardiac anomalies, seizures, and visual abnormalities (including cortical visual impairment and microphthalmia). One female with the p.Arg83Cys variant and one female with an NAA15 frameshift variant both have microphthalmia. The frameshift variants located toward the C-terminal end of NAA10 have much less impact on overall functioning, whereas the females with the p.Arg83Cys missense in NAA10 have substantial impairment. The overall data are consistent with a phenotypic spectrum for these alleles, involving multiple organ systems, thus revealing the widespread effect of alterations of the NTA pathway in humans.


Subject(s)
Autism Spectrum Disorder , Intellectual Disability , Microphthalmos , Humans , Female , Syndrome , N-Terminal Acetyltransferase E/genetics , N-Terminal Acetyltransferase E/metabolism , Genotype , Intellectual Disability/genetics , N-Terminal Acetyltransferase A/genetics , N-Terminal Acetyltransferase A/metabolism
2.
Pediatr Dev Pathol ; 25(6): 611-623, 2022.
Article in English | MEDLINE | ID: mdl-36120950

ABSTRACT

Background: Myhre syndrome, caused by pathogenic variants in SMAD4, is characterized by compact body habitus with short stature, distinctive craniofacial appearance, stiff skin, cardiovascular abnormalities (valve stenosis, coarctation, hypoplasia, or stenosis of aorta), effusions of potential spaces (pericardium, pleura, peritoneum), restricted movement of the joints (including thorax), and hearing loss. Lung and airway disease has been reported, but not always well-defined, to include interstitial lung disease, large airway obstruction, and pulmonary arterial hypertension. Excessive fibroproliferation of tissues especially following trauma or surgical instrumentation has been recognized, although these may also present spontaneously. Method: We report the pathologic features of 1 new patient with progressive choanal stenosis, and 22 literature cases, including the expanded history of 5 patients (3 who died). Results: Examination of patient tissues documents cellular fibroproliferation and deposition of excessive extracellular matrix explaining some of the observed clinical features of Myhre syndrome. Conclusion: Excessive fibrosis is noted in multiple tissues, especially heart, lung, and upper and lower airways. Our research provides the first systematic review to provide a knowledge base of gross and pathologic findings in Myhre syndrome.


Subject(s)
Gain of Function Mutation , Hand Deformities, Congenital , Male , Humans , Constriction, Pathologic , Hand Deformities, Congenital/diagnosis , Hand Deformities, Congenital/pathology , Facies , Smad4 Protein/genetics
3.
Clin Genet ; 100(4): 468-477, 2021 10.
Article in English | MEDLINE | ID: mdl-34212383

ABSTRACT

We describe the clinical features of nine unrelated individuals with rare de novo missense or in-frame deletions/duplications within the "HX motif" of exon 7 of ATN1. We previously proposed that individuals with such variants should be considered as being affected by the syndromic condition of congenital hypotonia, epilepsy, developmental delay, and digital anomalies (CHEDDA), distinct from dentatorubral-pallidoluysian atrophy (DRPLA) secondary to expansion variants in exon 5 of ATN1. We confirm that the universal phenotypic features of CHEDDA are distinctive facial features and global developmental delay. Infantile hypotonia and minor hand and feet differences are common and can present as arthrogryposis. Common comorbidities include severe feeding difficulties, often requiring gastrostomy support, as well as visual and hearing impairments. Epilepsy and congenital malformations of the brain, heart, and genitourinary systems are frequent but not universal. Our study confirms the clinical entity of CHEDDA secondary to a mutational signature restricted to exon 7 of ATN1. We propose a clinical schedule for assessment upon diagnosis, surveillance, and early intervention including the potential of neuroimaging for prognostication.


Subject(s)
Genetic Predisposition to Disease , Mutation , Nerve Tissue Proteins/genetics , Neurodevelopmental Disorders/diagnosis , Neurodevelopmental Disorders/genetics , Phenotype , Child, Preschool , Facies , Female , Genetic Association Studies , Humans , Male , Syndrome
6.
Am J Cardiol ; 140: 118-121, 2021 02 01.
Article in English | MEDLINE | ID: mdl-33144168

ABSTRACT

Patients with the Turner syndrome (TS) often have longer QT intervals compared with age-matched peers although the significance of this remains unknown. We sought to determine the degree, frequency and impact of QTc prolongation in patients with TS. A chart review of all patients with an electrocardiogram (ECG) and genetically proven TS was performed. Medications at the time of the ECG were reviewed and QTc calculated. Medications were classified according to QTc risk using www.crediblemeds.com. ECG parameters were compared with an age, gender, and cardiac lesion-matched control group. Over the 10-year period of review, 112 TS patients with a mean age of 34 ± 25 years underwent 226 ECGs. At least 1 QTc prolonging medication was prescribed in 81 (74%) patients. Longer QTc interval correlated with absence of y chromosomal material (p = 0.01), older age (p <0.0001), increased number of QTc prolonging and nonprolonging medications (p <0.0001 each). During the 7.0 ± 5.1 years of follow-up, no patient had ventricular arrhythmia or unexplained sudden death. QTc was significantly shorter in matched controls using either Bazett or Hodges formula (424 ± 16 ms vs 448 ± 28 ms, p <0.0001; and 414.8 ± 16 ms vs 424.2 ± 20 ms; p = 0.0002, respectively). However, there was no difference in the frequency of QTc prolongation >460 msec (2.8% vs 2.6%, p = 0.9). In conclusion, despite frequent use of QT-prolonging medications, ventricular arrhythmias are rare in TS.


Subject(s)
Electrocardiography , Heart Rate/physiology , Long QT Syndrome/etiology , Turner Syndrome/complications , Adult , Female , Follow-Up Studies , Humans , Long QT Syndrome/diagnosis , Long QT Syndrome/physiopathology , Male , Prognosis , Retrospective Studies , Turner Syndrome/diagnosis , Turner Syndrome/physiopathology , Young Adult
7.
Int J Cardiol ; 325: 127-131, 2021 02 15.
Article in English | MEDLINE | ID: mdl-33045278

ABSTRACT

BACKGROUND: The frequency of ascending aortic dissection in patients with Turner syndrome in the United States remains largely unknown with data surmised from published case reports or case series. Dissection of other vascular structures has only rarely been reported in this patient cohort. Recent European data identified aortic dissection to be a relatively rare event in a group of adult women with Turner syndrome. We sought to evaluate the prevalence of, and risk factors for, vascular dissection in women with Turner syndrome followed in the United States. METHOD: Retrospective review of all adult patients (age > 18 years) with Turner syndrome seen by any medical care provider within 2 medical systems covering a 5 state referral base was performed. Demographic, clinical, surgical and imaging variables of interest were recorded. RESULTS: Vascular dissection occurred in 16 (4.1%) of the 393 adult women and prophylactic aortic replacement occurred in 14 (3.5%). Only 35% of patients were under the care of a cardiologist with the remainder followed exclusively by other care providers. Vascular dissections occurred in the ascending & descending aorta as well as pulmonary artery and cerebral vessels. In addition to bicuspid aortic valve, and prior cardiac surgery, risk factors for vascular dissection included rural residence and lack of ongoing care by a cardiologist. CONCLUSION: Transition to adult cardiology subspecialty care is lacking in patients with Turner syndrome. Aortic dissection is not uncommon. Ongoing interaction with a cardiologist is essential to optimize cardiac outcomes in those with cardiac risk factors and may best be accomplished with centralized multidisciplinary clinics.


Subject(s)
Aortic Dissection , Turner Syndrome , Adult , Aortic Dissection/diagnostic imaging , Aortic Dissection/epidemiology , Aortic Dissection/etiology , Aorta , Dissection , Female , Humans , Middle Aged , Retrospective Studies , Turner Syndrome/complications , Turner Syndrome/diagnosis , Turner Syndrome/epidemiology
9.
Am J Med Genet A ; 182(2): 328-337, 2020 02.
Article in English | MEDLINE | ID: mdl-31837202

ABSTRACT

Myhre syndrome is an increasingly diagnosed rare syndrome that is caused by one of two specific heterozygous gain-of-function pathogenic variants in SMAD4. The phenotype includes short stature, characteristic facial appearance, hearing loss, laryngotracheal stenosis, arthritis, skeletal abnormalities, learning and social challenges, distinctive cardiovascular defects, and a striking fibroproliferative response in the ear canals, airways, and serosal cavities (peritoneum, pleura, pericardium). Confirmation of the clinical diagnosis is usually prompted by the characteristic appearance with developmental delay and autistic-like behavior using targeted gene sequencing or by whole exome sequencing. We describe six patients (two not previously reported) with molecularly confirmed Myhre syndrome and neoplasia. Loss-of-function pathogenic variants in SMAD4 cause juvenile polyposis syndrome and we hypothesize that the gain-of-function pathogenic variants observed in Myhre syndrome may contribute to neoplasia in the patients reported herein. The frequency of neoplasia (9.8%, 6/61) in this series (two new, four reported patients) and endometrial cancer (8.8%, 3/34, mean age 40 years) in patients with Myhre syndrome, raises the possibility of cancer susceptibility in these patients. We alert clinicians to the possibility of detecting this syndrome when cancer screening panels are used. We propose that patients with Myhre syndrome are more susceptible to neoplasia, encourage increased awareness, and suggest enhanced clinical monitoring.


Subject(s)
Cryptorchidism/genetics , Endometrial Neoplasms/genetics , Growth Disorders/genetics , Hand Deformities, Congenital/genetics , Intellectual Disability/genetics , Neoplasms/genetics , Smad4 Protein/genetics , Adult , Cryptorchidism/complications , Cryptorchidism/pathology , Endometrial Neoplasms/complications , Endometrial Neoplasms/pathology , Facies , Female , Gain of Function Mutation/genetics , Growth Disorders/complications , Growth Disorders/pathology , Hand Deformities, Congenital/complications , Hand Deformities, Congenital/pathology , Heterozygote , Humans , Intellectual Disability/complications , Intellectual Disability/pathology , Male , Middle Aged , Mutation/genetics , Neoplasms/complications , Neoplasms/pathology , Phenotype , Transforming Growth Factor beta/genetics , Exome Sequencing
10.
World J Pediatr Congenit Heart Surg ; 11(4): NP144-NP147, 2020 Jul.
Article in English | MEDLINE | ID: mdl-29793379

ABSTRACT

Kawasaki disease can be difficult to diagnose in infants, putting them at higher risk for developing coronary artery dilatation. It can be even more difficult to diagnose in the setting of preexisting cardiac anomalies such as those found in Williams syndrome. We present a case of a three-month-old male with Williams syndrome with rapidly developing giant coronary aneurysms due to Kawasaki disease. This case demonstrates the importance of repeat echocardiography in diagnosing incomplete Kawasaki disease in infants. We speculate that elastin changes, as present in Williams syndrome, may put affected children at higher risk for development of giant coronary arteries should they acquire Kawasaki disease.


Subject(s)
Coronary Aneurysm/etiology , Mucocutaneous Lymph Node Syndrome/diagnosis , Williams Syndrome/diagnosis , Coronary Aneurysm/diagnosis , Echocardiography , Humans , Infant , Male , Mucocutaneous Lymph Node Syndrome/complications , Tomography, X-Ray Computed , Williams Syndrome/complications
11.
Hemoglobin ; 43(3): 207-209, 2019 May.
Article in English | MEDLINE | ID: mdl-31387435

ABSTRACT

We describe here a previously unreported hemoglobin (Hb) variant, Hb Gibbon [ß124(H2)Pro→Thr (HBB: c.373C>A, p.P125T)] detected by newborn Hb screening in a term male with no family history for hemoglobinopathy or other screening abnormalities. This missense mutation produces a ß-globin chain variant that was detected by high performance liquid chromatography (HPLC) methods, but is silent by capillary electrophoresis (CE). DNA sequencing studies revealed that his father was also a heterozygote for this mutation. Neither has abnormalities on complete blood count (CBC) or any symptomatology.


Subject(s)
Alleles , Amino Acid Substitution , Asymptomatic Diseases , Hemoglobinopathies/diagnosis , Hemoglobinopathies/genetics , beta-Globins/genetics , Chromatography, High Pressure Liquid , DNA Mutational Analysis , Genotype , Hemoglobins, Abnormal/genetics , Humans , Infant, Newborn , Neonatal Screening , beta-Globins/analysis , beta-Globins/metabolism
12.
Congenit Heart Dis ; 14(5): 864-867, 2019 Sep.
Article in English | MEDLINE | ID: mdl-31328377

ABSTRACT

OBJECTIVES: This study assessed the frequency and utility of echocardiographic examination in patients with all forms of Ehlers-Danlos syndrome and sought to identify clinical variables associated with an abnormal echocardiogram. DESIGN/SETTING: This was a retrospective study of all patients carrying a diagnosis of Ehlers-Danlos syndrome of any type who were evaluated by a pediatrician or pediatric subspecialist at a single tertiary medical center with an affiliated children's hospital during the period January 2013 to December 2018. PATIENTS: Chart review was performed on all patients carrying a diagnosis of Ehlers-Danlos syndrome in the electronic medical record. OUTCOME MEASURES: Data from genetics examination, cardiovascular examination where applicable, genetic test results when available, and echocardiography were recorded. RESULTS: Of 262 patients identified, echocardiography and cardiac evaluation were common occurring in 90% and 50% of patients with any form of Ehlers-Danlos syndrome. Cardiovascular complications occurred in 50% of patients with vascular Ehlers-Danlos syndrome but echocardiography was normal in all. Aortic dilation was common in classic Ehlers-Danlos syndrome but absent in hypermobile Ehlers-Danlos syndrome. Mitral valve prolapse and bicuspid aortic valve occurred at the same incidence as the general population. Cardiac symptoms were present in 12% but did not correlate with abnormal cardiac structure. Presentation with symptoms of musculoskeletal pain was inversely related to the presence of cardiac pathology. CONCLUSIONS: In light of the absence of cardiac pathology in patients with hypermobile Ehlers-Danlos syndrome, routine cardiac evaluation and echocardiography are not required for patients with hypermobile Ehlers-Danlos syndrome.


Subject(s)
Echocardiography/statistics & numerical data , Ehlers-Danlos Syndrome/diagnosis , Heart Diseases/diagnosis , Heart Ventricles/diagnostic imaging , Child , Diagnosis, Differential , Ehlers-Danlos Syndrome/complications , Female , Heart Diseases/etiology , Humans , Male , Reproducibility of Results , Retrospective Studies
13.
Am J Med Genet A ; 179(7): 1270-1275, 2019 07.
Article in English | MEDLINE | ID: mdl-31148362

ABSTRACT

PIGQ (OMIM *605754) encodes phosphatidylinositol glycan biosynthesis class Q (PIGQ) and is required for proper functioning of an N-acetylglucosamine transferase complex in a similar manner to the more established PIGA, PIGC, and PIGH. There are two previous patients reported with homozygous and apparently deleterious PIGQ mutations. Here, we provide the first detailed clinical report of a patient with heterozygous deleterious mutations associated with glycosylphosphatidylinositol-anchored protein (GPI-AP) biosynthesis deficiency. Our patient died at 10 months of age. The rare skeletal findings in this disorder expand the differential diagnosis of long bone radiolucent lesions and sphenoid wing dysplasia. This clinical report describes a new and rare disorder-PIGQ GPI-AP biosynthesis deficiency syndrome.


Subject(s)
Abnormalities, Multiple/genetics , Bone Diseases, Developmental/genetics , Glycosylphosphatidylinositols/deficiency , Membrane Proteins/genetics , Muscle Hypotonia/genetics , Mutation , Seizures/genetics , Abnormalities, Multiple/diagnosis , Abnormalities, Multiple/metabolism , Abnormalities, Multiple/pathology , Bone Diseases, Developmental/diagnosis , Bone Diseases, Developmental/metabolism , Bone Diseases, Developmental/pathology , Fatal Outcome , Gene Expression , Glycosylphosphatidylinositols/genetics , Glycosylphosphatidylinositols/metabolism , Heterozygote , Humans , Infant , Male , Membrane Proteins/deficiency , Muscle Hypotonia/diagnosis , Muscle Hypotonia/metabolism , Muscle Hypotonia/pathology , Phenotype , Seizures/diagnosis , Seizures/metabolism , Seizures/pathology , Sphenoid Bone/metabolism , Sphenoid Bone/pathology , Syndrome , Exome Sequencing
14.
Am J Med Genet A ; 179(5): 808-812, 2019 05.
Article in English | MEDLINE | ID: mdl-30838730

ABSTRACT

ARID2 loss-of-function is associated with a rare genetic disorder characterized in 14 reported patients to date. ARID2 encodes a member of the SWItch/sucrose non-fermentable chromatin remodeling complex. Other genes encoding subunits of this complex, such as ARID1A, ARID1B, and SMARCA2, are mutated in association with Coffin-Siris syndrome (CSS) and Nicolaides Baraitser syndrome (NCBRS) phenotypes. Previously reported ARID2 mutations manifested clinically with a CSS-like phenotype including intellectual disability, coarsened facial features, fifth toenail hypoplasia, and other recognizable dysmorphisms. However, heterogeneity exists between previously reported patients with some patients showing more overlapping features with NCBRS. Herein, we present a patient with a novel disease-causing ARID2 loss-of-function mutation. His clinical features included intellectual disability, coarse and dysmorphic facial features, toenail hypoplasia, ADHD, short stature, and delayed development consistent with prior reports. Our patient also presented with previously unreported clinical findings including ophthalmologic involvement, persistent fetal fingertip and toetip pads, and diffuse hyperpigmentary and hypopigmentary changes sparing his face, palms, and soles. The anomalous skin findings are particularly of interest given prior literature outlining the role of ARID2 in melanocyte homeostasis and melanoma. This clinical report and review of the literature is further affirming of the characteristic symptoms and expands the phenotype of this newly described and rare syndrome.


Subject(s)
Genetic Predisposition to Disease , Intellectual Disability/diagnosis , Intellectual Disability/genetics , Loss of Function Mutation , Phenotype , Skin Pigmentation/genetics , Transcription Factors/genetics , Child , Chromosomal Proteins, Non-Histone , Facies , Genetic Association Studies , Genetic Variation , Humans , Male , Radiography
15.
World J Pediatr Congenit Heart Surg ; 10(3): 376-379, 2019 05.
Article in English | MEDLINE | ID: mdl-28673110

ABSTRACT

Aortic aneurysms requiring surgery in early childhood are rare. Herein we describe the case of a three-year-old with massive aneurysmal aortic dilation secondary to the rare and often lethal genetic disorder, cutis laxa. Initial thoracic aortic aneurysm gene panel was negative. Parents of the child were not known to be consanguineous, but high-density SNP array revealed several regions of homozygosity. This prompted targeted sequence analysis that identified a novel homozygous missense mutation in the gene for cutis laxa, EFEMP2. The patient underwent aortic valve-sparing aortic root and ascending aorta replacement and total aortic arch replacement, with continuous, moderately hypothermic cardiopulmonary bypass, using a dual cannulation technique. He was discharged well on the third postoperative day and remains free of aneurysmal disease at two-year follow-up.


Subject(s)
Aorta/surgery , Aortic Aneurysm, Thoracic/surgery , Aortic Valve/surgery , Blood Vessel Prosthesis Implantation/methods , Cutis Laxa/complications , Aorta/diagnostic imaging , Aortic Aneurysm, Thoracic/diagnosis , Aortic Aneurysm, Thoracic/etiology , Aortic Valve/diagnostic imaging , Child, Preschool , Computed Tomography Angiography , Echocardiography , Humans , Imaging, Three-Dimensional , Male
17.
Am J Med Genet A ; 176(4): 1011-1014, 2018 04.
Article in English | MEDLINE | ID: mdl-29575632

ABSTRACT

We describe a neonatal patient with fixed dilated pupils and pulmonary, bladder, and bowel dysfunction suspicious for the presence of ACTA2 R179 mediated multisystemic smooth muscle dysfunction syndrome. Whole exome sequencing revealed compound heterozygous mutations in MYH11 after ACTA2 specific testing revealed no abnormalities. The child lived until 18 months of age and represents the only reported case of an MYH11 compound heterozygote with widespread smooth muscle dysfunction.


Subject(s)
Abnormalities, Multiple/diagnosis , Abnormalities, Multiple/genetics , Genes, Recessive , Muscle, Smooth/physiopathology , Mutation , Myosin Heavy Chains/genetics , Phenotype , Alleles , Amino Acid Substitution , DNA Mutational Analysis , Diagnostic Imaging , Fatal Outcome , Genetic Association Studies , Heterozygote , Humans , Infant , Male , Syndrome
18.
J Spec Pediatr Nurs ; 23(2): e12211, 2018 04.
Article in English | MEDLINE | ID: mdl-29473279

ABSTRACT

PURPOSE: Advances in genomic technology and research have led to genetic testing being recognized as an essential component of the etiological workup for children with autism spectrum disorder (ASD). Chromosomal microarray analysis (CMA) is a first-tier diagnostic test for patients with ASD, as recommended by the American College of Medical Genetics and other professional societies. An accurate underlying medical diagnosis for ASD has many potential benefits, including appropriate medical management, detailed therapeutic recommendations, and accurate recurrence risk. Genetic testing is relatively complicated, expensive, and, currently, in the majority of the cases, does not provide any organic improvement in the management of symptoms. DESIGN AND METHODS: We conducted semistructured interviews with 20 parents to explore the decision-making process of genetic testing from the perspectives and experiences of parents of children with ASD. Data were analyzed using qualitative content analysis. RESULTS: Parents had limited knowledge of genetic testing for ASD prior to a genetics clinic visit. The majority of the participants thought genetic testing would be beneficial for their child, their reproductive choices, and potential future generations. PRACTICE IMPLICATIONS: Various stakeholders (geneticists, primary care providers, nurses, and families) would benefit from future establishment of educational strategies to inform parental decision-making regarding genetic testing for children with ASD.


Subject(s)
Autism Spectrum Disorder/genetics , Decision Making , Genetic Predisposition to Disease/epidemiology , Genetic Testing/methods , Parents/psychology , Adolescent , Autism Spectrum Disorder/diagnosis , Child , Child, Preschool , Female , Health Knowledge, Attitudes, Practice , Humans , Interviews as Topic , Male , Perception , Qualitative Research , Risk Assessment
19.
Am J Med Genet A ; 170(9): 2416-20, 2016 09.
Article in English | MEDLINE | ID: mdl-27338032

ABSTRACT

Duplications of the long arm of chromosome 6 have been previously reported in a limited number of patients; however, most reported duplications encompass regions of chromosome 6 distal to band q21. Duplications restricted to the proximal portion of 6q are rare. We report an 8-year-old male with a 16.4 megabase (Mb) tandem duplication of chromosome 6q14.1q16.1 (chr6:78950191-95395865; hg19) who exhibited dysmorphic facial features, seizures, global developmental delay, intellectual disability, autism spectrum disorder, sensorineural hearing loss, and immune deficiency. This patient refines and potentially expands the current, poorly-characterized phenotype associated with duplication of this proximal 6q region. We recommend a low threshold for a hearing evaluation beyond newborn screening and for pursuing an immune work-up in patients with similar 6q duplications. © 2016 Wiley Periodicals, Inc.


Subject(s)
Chromosome Duplication , Chromosomes, Human, Pair 6 , Genetic Association Studies , Phenotype , Tandem Repeat Sequences , Abnormalities, Multiple , Child , Chromosome Banding , Comparative Genomic Hybridization , Facies , Genotype , Humans , Male , Oligonucleotide Array Sequence Analysis , Polymorphism, Single Nucleotide
20.
Am J Med Genet A ; 167A(12): 2893-901, 2015 Dec.
Article in English | MEDLINE | ID: mdl-26420300

ABSTRACT

Myhre syndrome, a connective tissue disorder characterized by deafness, restricted joint movement, compact body habitus, and distinctive craniofacial and skeletal features, is caused by heterozygous mutations in SMAD4. Cardiac manifestations reported to date have included patent ductus arteriosus, septal defects, aortic coarctation and pericarditis. We present five previously unreported patients with Myhre syndrome. Despite varied clinical phenotypes all had significant cardiac and/or pulmonary pathology and abnormal wound healing. Included herein is the first report of cardiac transplantation in patients with Myhre syndrome. A progressive and markedly abnormal fibroproliferative response to surgical intervention is a newly delineated complication that occurred in all patients and contributes to our understanding of the natural history of this disorder. We recommend routine cardiopulmonary surveillance for patients with Myhre syndrome. Surgical intervention should be approached with extreme caution and with as little invasion as possible as the propensity to develop fibrosis/scar tissue is dramatic and can cause significant morbidity and mortality.


Subject(s)
Cryptorchidism/etiology , Cryptorchidism/therapy , Growth Disorders/etiology , Growth Disorders/therapy , Hand Deformities, Congenital/etiology , Hand Deformities, Congenital/therapy , Heart Diseases/surgery , Intellectual Disability/etiology , Intellectual Disability/therapy , Child , Cryptorchidism/complications , Electrocardiography , Facies , Female , Growth Disorders/complications , Hand Deformities, Congenital/complications , Heart Transplantation , Humans , Intellectual Disability/complications , Male , Mutation , Pregnancy , Smad4 Protein/genetics , Young Adult
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