منابع مشابه
Autism and tuberous sclerosis.
Autism is a behavior disorder with genetic influences indicated from twin and family studies and from the co-occurrence of autism with known genetic disorders. Tuberous sclerosis complex (TSC) is a known genetic disorder with behavioral manifestations including autism. A literature review of these two disorders substantiates a significant association of autism and TSC with 17-58% of TSC subject...
متن کاملAutism in Tuberous Sclerosis
A case of Tuberous Sclerosis with infantile autism, misdiagnosed as mental retardation with seizure disorder is being discussed in light of the implication of the misdiagnosis.
متن کاملTuberous Sclerosis Complex in Autism
OBJECTIVE To study the prevalence rate of tuberous sclerosis complex in autistic disorder. METHODS We studied one cohort of children followed up since 2005 until 2009, with autistic disorder, to determine the incidence of tuberous sclerosis complex. We established an autistic disorder registry in 2005 at China Rehabilitation Research Center. During the 4-year period (2005-2009), we collected ...
متن کاملTuberous sclerosis.
Tuberous sclerosis - also called tuberous sclerosis complex (TSC) - is a rare, multi-system genetic disorder affecting cellular differentiation & proliferation, which results in hamartoma formation in many organs. The classic triad of clinical features comprises mental retardation, epilepsy & skin lesion, but these three features are not always present. Mrs. Jahanara Khatun, a 30 years old lady...
متن کاملtuberous sclerosis
A search for children presenting with signs or symptoms of cardiac rhabdomyomas was made through members of the paediatric section of the British Cardiac Society in order to establish their birth incidence, presenting features, clinical course, and the frequency of a concurrent diagnosis of tuberous sclerosis. Fifteen children were identified and 12 had tuberous sclerosis (80%). Heart failure w...
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ژورنال
عنوان ژورنال: Journal of Autism and Developmental Disorders
سال: 1992
ISSN: 0162-3257,1573-3432
DOI: 10.1007/bf01048239