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2.
Am J Med Genet A ; 158A(10): 2591-601, 2012 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-22903861

RESUMO

We identified a novel 6.33 Mb deletion of 1q21.3q23.3 (hg18; chr1: 153035245-159367106) in two siblings presenting with blepharophimosis, ptosis, microbrachycephaly, severe psychomotor, and intellectual disability. Additional common features include small corpus callosum, normal birth length and head circumference, postnatal growth restriction, low anterior hairline, upturned nose, bilateral preauricular pits, widely spaced teeth, gingival hypertrophy, left ventricular dilatation with decreased biventricular systolic function, delayed bone age, 5th finger clinodactyly, short 3rd digit, hyperconvex nails, obstructive and central sleep apnea, and bilateral heel contractures. Fluorescence in situ hybridization (FISH) performed in the mother of both children showed an apparently balanced, intrachromosomal insertional translocation of 1q21.3q23.3 to 1q42.12. The sibling recurrence likely arose by a maternal meiotic crossing over on the rearranged chromosome 1 between the deleted region and the insertion. We hypothesize that the decreased cardiac function and contractures may be related to LMNA haploinsufficiency. This case illustrates the importance of FISH when attempting to determine inheritance of a copy-number variation and emphasize the value of evaluating known haploinsufficiency phenotypes for genes in deleted regions.


Assuntos
Deleção Cromossômica , Cromossomos Humanos Par 1/genética , Irmãos , Translocação Genética , Anormalidades Múltiplas/genética , Anormalidades Múltiplas/patologia , Adolescente , Blefarofimose/genética , Blefarofimose/patologia , Blefaroptose/genética , Blefaroptose/patologia , Criança , Deficiências do Desenvolvimento/genética , Deficiências do Desenvolvimento/patologia , Feminino , Cardiopatias Congênitas/genética , Cardiopatias Congênitas/patologia , Humanos , Hibridização in Situ Fluorescente , Deficiência Intelectual/genética , Deficiência Intelectual/patologia , Masculino , Mutagênese Insercional
3.
Birth Defects Res A Clin Mol Teratol ; 88(5): 263-85, 2010 May.
Artigo em Inglês | MEDLINE | ID: mdl-20506459

RESUMO

BACKGROUND: The 49-year history of the Teratology Society is reviewed. An abbreviated history is outlined in table form, with listings of the Warkany Lectures, the Continuing Education Courses, and officers of the society. The original article was updated to include the years 2000 to 2010. METHODS: A year-by-year description of the events is given, including the scientific and social content of the annual meetings and changes in the business of the society, in many cases using comments from the past presidents. The valuable and unique diversity of the members is discussed and illustrated, presenting the disciplines and main research areas of the presidents. The number of submitted abstracts and the various categories are tabulated, averaging the number and type over successive periods. A significant increase in the number of abstracts dealing with epidemiology and developmental biology is evident. The society's development is compared to that of a human, and the question was asked by Shephard et al. (2000): Have we reached the maturational stage of old age or senescence, or is the society still maturing gracefully? This question needs further discussion by all the members. By 2010, many positive changes are happening to revitalize the society. RESULTS: During the past 50 years, we have developed the scientific basis to prevent birth defects caused by rubella, alcoholism, and folate deficiency, as well as other prenatal exposures. We are now taking advantage of advances in many fields to begin shaping the Teratology Society of the 21st century. CONCLUSIONS: We must now engage in political battles to obtain the resources needed to conduct further research and to implement prevention programs, as well as to provide care and rehabilitation for persons with birth defects.


Assuntos
Sociedades Médicas , Teratologia
4.
Birth Defects Res A Clin Mol Teratol ; 85(8): 710-4, 2009 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-19441097

RESUMO

A paper published in 1925 reported that human fetuses with anencephaly have arms that are longer than normal. This finding was accepted as true through the early 1990s. An analysis of body dimensions done in 1996 and enlarged and updated here shows that the arms of human fetuses with anencephaly are appropriate for gestational age and normal in proportion to their leg lengths. A subtle difference in measurement technique was found to explain the discordant findings.


Assuntos
Anencefalia/patologia , Braço/anormalidades , Braço/diagnóstico por imagem , Ultrassonografia Pré-Natal/métodos , Anencefalia/diagnóstico por imagem , Braço/embriologia , Feminino , Feto/anormalidades , Feto/anatomia & histologia , Feto/embriologia , Humanos , Perna (Membro)/anormalidades , Perna (Membro)/diagnóstico por imagem , Perna (Membro)/embriologia , Gravidez , Diagnóstico Pré-Natal
8.
Prenat Diagn ; 25(6): 442-7, 2005 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-15966043

RESUMO

OBJECTIVES: To describe the prenatal imaging findings in fetuses at risk for Joubert syndrome (JS), review the literature and propose a protocol for prenatal diagnosis of JS using ultrasound and MRI. METHODS: We reviewed prenatal ultrasound and fetal MRI studies in two pregnancies at 25% recurrence risk for JS and correlated these findings with gross neuropathology in one affected fetus. RESULTS: While abnormalities such as occipital encephalocele or enlarged cisterna magna have been identified before mid-trimester, the definitive diagnosis of JS, based on core cerebellar findings, has only been possible after 17 weeks' gestation. CONCLUSIONS: With longitudinal monitoring, it is possible to diagnose JS in at-risk pregnancies before 24 weeks' gestation. On the basis of our data and review of the literature, we propose a protocol for monitoring pregnancies at risk for JS, utilizing serial ultrasounds combined with fetal MRI at 20-22 weeks' gestation to maximize the accuracy of prenatal diagnosis.


Assuntos
Cerebelo/anormalidades , Imageamento por Ressonância Magnética , Diagnóstico Pré-Natal/métodos , Ultrassonografia Pré-Natal , Ataxia , Movimentos Oculares , Feminino , Idade Gestacional , Humanos , Deficiência Intelectual , Masculino , Gravidez , Fatores de Risco , Síndrome
9.
Hum Mutat ; 23(2): 147-159, 2004 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-14722918

RESUMO

We recently identified mutations of ARX in nine genotypic males with X-linked lissencephaly with abnormal genitalia (XLAG), and in several female relatives with isolated agenesis of the corpus callosum (ACC). We now report 13 novel and two recurrent mutations of ARX, and one nucleotide change of uncertain significance in 20 genotypic males from 16 families. Most had XLAG, but two had hydranencephaly and abnormal genitalia, and three males from one family had Proud syndrome or ACC with abnormal genitalia. We obtained detailed clinical information on all 29 affected males, including the nine previously reported subjects. Premature termination mutations consisting of large deletions, frameshifts, nonsense mutations, and splice site mutations in exons 1 to 4 caused XLAG or hydranencephaly with abnormal genitalia. Nonconservative missense mutations within the homeobox caused less severe XLAG, while conservative substitution in the homeodomain caused Proud syndrome. A nonconservative missense mutation near the C-terminal aristaless domain caused unusually severe XLAG with microcephaly and mild cerebellar hypoplasia. In addition, several less severe phenotypes without malformations have been reported, including mental retardation with cryptogenic infantile spasms (West syndrome), other seizure types, dystonia or autism, and nonsyndromic mental retardation. The ARX mutations associated with these phenotypes have included polyalanine expansions or duplications, missense mutations, and one deletion of exon 5. Together, the group of phenotypes associated with ARX mutations demonstrates remarkable pleiotropy, but also comprises a nearly continuous series of developmental disorders that begins with hydranencephaly, lissencephaly, and agenesis of the corpus callosum, and ends with a series of overlapping syndromes with apparently normal brain structure.


Assuntos
Regulação da Expressão Gênica/genética , Proteínas de Homeodomínio/genética , Mutação/genética , Fatores de Transcrição/genética , Anormalidades Múltiplas/genética , Anormalidades Múltiplas/patologia , Agenesia do Corpo Caloso , Células Cultivadas , Corpo Caloso/patologia , Análise Mutacional de DNA/métodos , Feminino , Ligação Genética/genética , Genitália Feminina/anormalidades , Genitália Feminina/patologia , Genitália Masculina/anormalidades , Genitália Masculina/patologia , Genótipo , Proteínas de Homeodomínio/biossíntese , Humanos , Recém-Nascido , Linfócitos/química , Linfócitos/metabolismo , Linfócitos/patologia , Imageamento por Ressonância Magnética , Masculino , Mutação de Sentido Incorreto/genética , Linhagem , Fenótipo , Transtornos dos Cromossomos Sexuais/genética , Fatores de Transcrição/biossíntese
10.
Pediatr Radiol ; 32(11): 778-82, 2002 11.
Artigo em Inglês | MEDLINE | ID: mdl-12389104

RESUMO

BACKGROUND: Asplenia syndrome is a form of heterotaxy characterized by bilateral right-sidedness. Congenital fusion of the adrenal glands ("horseshoe adrenal gland") is a less common feature of asplenia syndrome, most instances of which have been found at autopsy. PURPOSE: To present clinical and imaging features of infants diagnosed with asplenia syndrome and horseshoe adrenal gland. MATERIALS AND METHODS: Six infants with asplenia syndrome were identified as having a horseshoe adrenal gland. Medical records and imaging studies were reviewed to determine clinical presentation, associated anomalies, and outcome. The literature was reviewed for prior reports of horseshoe adrenal gland. RESULTS: Horseshoe adrenal gland was identified in five infants by sonography and one by CT, the latter confirmed by autopsy. In all cases, the horseshoe adrenal gland was pre-aortic. Besides features of asplenia syndrome, one infant also had associated vertebral anomalies and bilateral renal agenesis. Including the current cases, of 65 reported cases of horseshoe adrenal gland 34 (52%) were associated with asplenia, 24 (37%) with neural tube defects, 19 (29%) with renal anomalies, and 2 (3%) with Cornelia de Lange syndrome. Horseshoe adrenal gland has not been reported with polysplenia syndrome. CONCLUSIONS: Horseshoe adrenal gland is a less common manifestation of asplenia that may be demonstrated by imaging. Horseshoe adrenal gland may be a differentiating feature between asplenia and polysplenia.


Assuntos
Glândulas Suprarrenais/anormalidades , Baço/anormalidades , Glândulas Suprarrenais/diagnóstico por imagem , Humanos , Recém-Nascido , Masculino , Baço/diagnóstico por imagem , Tomografia Computadorizada por Raios X , Ultrassonografia
11.
Am J Med Genet ; 112(1): 28-30, 2002 Sep 15.
Artigo em Inglês | MEDLINE | ID: mdl-12239716

RESUMO

Holoprosencephaly is associated with a diagnostic face approximately 80% of the time. We report three siblings with alobar holoprosencephaly and essentially normal faces. A similar family was reported by Khan et al. [1970: Dev Med Child Neurol 12:71-76]. Alobar holoprosencephaly with essentially normal faces has also been observed in infants of diabetic mothers [Barr et al., 1983: J Pediatr 102:565-568].


Assuntos
Face , Genes Recessivos , Holoprosencefalia/patologia , Evolução Fatal , Feminino , Holoprosencefalia/genética , Humanos , Lactente , Recém-Nascido , Masculino
12.
Teratology ; 66(2): 65-72, 2002 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-12210009

RESUMO

BACKGROUND: A female fetus with massive truncal-limb hydrops and large, loculated, nuchal hygromas in midgestation is highly likely to have Turner syndrome. This phenotype is recognized to be usually lethal, with only more mildly affected fetuses surviving to term birth. METHODS: The morphology and morphometrics of 117 midgestation fetuses with phenotypic Turner syndrome were analyzed. RESULTS: More than 90% of fetuses with phenotypic Turner syndrome were found to have heart weights below the 2.5 centile, as well as lung hypoplasia and restricted limb growth for brain weight standards, although brain weight was only mildly reduced for gestational age. In contrast, subnormal heart weight was much less common among fetuses with other etiologies of hydrops, hygromas, or pleural effusions. CONCLUSIONS: We hypothesize that myocardial hypoplasia is a primary defect in Turner syndrome, and it leads to or is a major contributor to the phenotypic features that end in midgestational death.


Assuntos
Morte Fetal/etiologia , Cardiopatias Congênitas/complicações , Síndrome de Turner/patologia , Feminino , Idade Gestacional , Cardiopatias Congênitas/diagnóstico por imagem , Humanos , Pulmão/anormalidades , Pulmão/diagnóstico por imagem , Tamanho do Órgão , Gravidez , Síndrome de Turner/diagnóstico por imagem , Ultrassonografia Pré-Natal
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