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1.
Neurol Sci ; 2024 Apr 12.
Article in English | MEDLINE | ID: mdl-38607533

ABSTRACT

BACKGROUND: SPG18 is caused by mutations in the endoplasmic reticulum lipid raft associated 2 (ERLIN2) gene. Autosomal recessive (AR) mutations are usually associated with complicated hereditary spastic paraplegia (HSP), while autosomal dominant (AD) mutations use to cause pure SPG18. AIM: To define the variegate clinical spectrum of the SPG18 and to evaluate a dominant negative effect of erlin2 (encoded by ERLIN2) on oligomerization as causing differences between AR and AD phenotypes. METHODS: In a four-generation pedigree with an AD pattern, a spastic paraplegia multigene panel test was performed. Oligomerization of erlin2 was analyzed with velocity gradient assay in fibroblasts of the proband and healthy subjects. RESULTS: Despite the common p.V168M mutation identified in ERLIN2, a phenoconversion to amyotrophic lateral sclerosis (ALS) was observed in the second generation, pure HSP in the third generation, and a complicated form with psychomotor delay and epilepsy in the fourth generation. Erlin2 oligomerization was found to be normal. DISCUSSION: We report the first AD SPG18 family with a complicated phenotype, and we ruled out a dominant negative effect of V168M on erlin2 oligomerization. Therefore, our data do not support the hypothesis of a relationship between the mode of inheritance and the phenotype, but confirm the multifaceted nature of SPG18 on both genetic and clinical point of view. Clinicians should be aware of the importance of conducting an in-depth clinical evaluation to unmask all the possible manifestations associated to an only apparently pure SPG18 phenotype. We confirm the genotype-phenotype correlation between V168M and ALS emphasizing the value of close follow-up.

2.
Neurocase ; 25(1-2): 62-65, 2019.
Article in English | MEDLINE | ID: mdl-30991884

ABSTRACT

Many neuropsychiatric phenotypes have been reported in association with rearrangements in the 15q11-q13 region. Clinical presentations can include hypotonia, developmental delay, severe/moderate intellectual disabilities, poor expressive language, difficult to treat epilepsy, and autism spectrum disorders. Here we report an additional case of a girl with inversion duplication on chromosome 15 (Inv-Dup 15) showing a peculiar and milder clinical phenotype, including atypical high-functioning autism disorder, late onset and drug-responsive epilepsy, and a relatively good language development . This report suggests that a diagnosis of Inv-Dup (15) can be suspected during more benign atypical condition with a better outcome than usually reported.


Subject(s)
Autism Spectrum Disorder/physiopathology , Epilepsy/physiopathology , Intellectual Disability/physiopathology , Adult , Autism Spectrum Disorder/etiology , Chromosome Aberrations , Chromosomes, Human, Pair 15 , Epilepsy/etiology , Female , Humans , Intellectual Disability/complications , Intellectual Disability/etiology
3.
Epilepsy Behav ; 56: 38-43, 2016 Mar.
Article in English | MEDLINE | ID: mdl-26827300

ABSTRACT

OBJECTIVE: The objective of this report was to assess the psychiatric comorbidity in a group of patients affected by autosomal dominant cortical tremor, myoclonus, and epilepsy (ADCME). METHODS: Reliable and validated psychodiagnostic scales including the BDI (Beck Depression Inventory), STAI-Y1 and 2 (State-Trait Anxiety Inventory - Y; 1 and 2), MMPI-2 (Minnesota Multiphasic Personality Inventory - 2), and QoLIE-31 (Quality of Life in Epilepsy Inventory - 31) were administered to 20 patients with ADCME, 20 patients with juvenile myoclonic epilepsy (JME), and 20 healthy controls. RESULTS: There was a higher prevalence of mood disorders in patients with ADCME compared to patients with JME and healthy controls, particularly depression (p=0.035 and p=0.017, respectively) and state anxiety (p=0.024 and p=0.019, respectively). Trait anxiety was not different from JME (p=0.102) but higher than healthy controls (p=0.017). The myoclonus score positively correlated with both state (rho: 0.58, p=0.042) and trait anxiety (rho: 0.65, p=0.011). These psychiatric features were also often associated with pathological traits of personality: paranoid (OR: 25.7, p=0.003), psychasthenia (OR: 7.0, p=0.023), schizophrenia (OR: 8.5, p=0.011), and hypomania (OR: 5.5, p=0.022). Finally, in patients with ADCME, decreased quality of life correlated with these psychiatric symptoms. SIGNIFICANCE: Patients with ADCME show a significant psychiatric burden that impairs their quality of life. A comprehensive psychiatric evaluation should be offered at the time of diagnosis to detect these comorbidities and to treat them.


Subject(s)
Epilepsy/psychology , Mental Disorders/psychology , Myoclonus/psychology , Tremor/psychology , Adult , Anxiety/epidemiology , Anxiety/psychology , Depression/epidemiology , Depression/psychology , Epilepsy/complications , Epilepsy/epidemiology , Female , Humans , Italy/epidemiology , Male , Mental Disorders/complications , Mental Disorders/epidemiology , Middle Aged , Mood Disorders/complications , Mood Disorders/epidemiology , Myoclonic Epilepsy, Juvenile/complications , Myoclonic Epilepsy, Juvenile/psychology , Myoclonus/complications , Myoclonus/epidemiology , Personality Disorders/epidemiology , Personality Disorders/psychology , Prevalence , Psychiatric Status Rating Scales , Psychotic Disorders/complications , Psychotic Disorders/epidemiology , Quality of Life , Tremor/complications , Tremor/epidemiology , Young Adult
4.
Brain Dev ; 38(7): 663-8, 2016 Aug.
Article in English | MEDLINE | ID: mdl-26897099

ABSTRACT

The widespread use of Array Comparative Genomic Hybridization (aCGH) technology has enabled the identification of several syndromes associated with copy number variants (CNVs) including the 17q21.31 microdeletion. The 17q21.31 microdeletion syndrome, also known as Koolen-de Vries syndrome, was first described in 2006 in individuals with intellectual disabilities and organ abnormalities. We report the clinical, instrumental, cytogenetic and molecular investigations of a boy admitted for epilepsy and intellectual disabilities. We carried out detailed analysis of the clinical phenotype of this patient and investigated the genetic basis by using aCGH. We identified a de novo microdeletion on chromosome 17q21.31, compatible with Koolen-de Vries syndrome. Our case shares some of the typical characteristics of the syndrome already described by other authors: delayed psychomotor development, primarily affecting the expressive language, dysmorphic facial features, and epilepsy. However the clinical outcome was not severe as the intellectual disabilities were moderate with good adaptive and functional behaviour. Epilepsy was easily controlled by a single drug, and he never needed surgery for organ abnormalities.


Subject(s)
Abnormalities, Multiple/genetics , Abnormalities, Multiple/physiopathology , Intellectual Disability/genetics , Intellectual Disability/physiopathology , Abnormalities, Multiple/diagnostic imaging , Abnormalities, Multiple/drug therapy , Adolescent , Brain/diagnostic imaging , Brain/physiopathology , Chromosome Deletion , Chromosomes, Human, Pair 17/genetics , Comparative Genomic Hybridization , Electroencephalography , Epilepsy/drug therapy , Epilepsy/genetics , Epilepsy/pathology , Epilepsy/physiopathology , Face/abnormalities , Humans , Intellectual Disability/diagnostic imaging , Intellectual Disability/drug therapy , Magnetic Resonance Imaging , Male , Nuclear Proteins/genetics , Parents , Phenotype , Receptors, Corticotropin-Releasing Hormone/genetics
5.
Epilepsia ; 54(5): e69-73, 2013 May.
Article in English | MEDLINE | ID: mdl-23448223

ABSTRACT

15q.13.3 microdeletion has been described in a variety of neurodevelopmental disorders. Epilepsy appears to be a common feature and, specifically, the 15q13.3 microdeletion is found in about 1% of patients with idiopathic generalized epilepsy. Recently, absence seizures with intellectual disability (ID) have been reported in patients carrying this mutation. We describe two families in which several affected members carry a 15q13.3 microdeletion in a pattern suggestive of autosomal dominant inheritance. Their phenotype includes mainly absence epilepsy and mild ID, suggesting only similarities with genetic/idiopathic generalized epilepsies but not typical features. The importance of studying such families is crucial to broaden the phenotype and understand the long-term outcome of patients with this condition.


Subject(s)
Chromosome Deletion , Chromosomes, Human, Pair 15/genetics , Epilepsy, Generalized/genetics , Genetic Predisposition to Disease , Adolescent , Adult , Electroencephalography , Epilepsy, Generalized/pathology , Family Health , Female , Humans , Intelligence , Italy , Magnetic Resonance Imaging , Male , Mutation
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