Tuberous sclerosis (TS) is a multiple-system disease involving the brain, skin, kidneys, heart and other visceral argans. There were 18 children with TS at our clinic, and complete studies of these patients and their families were performed. Male to female ratio was 11:7. Age at diagnosis was from 1 month to 18 years. Seizures (infantile spasm, generalized and partial epilepsy), skin lesions and intracranial calcifications were the most common clinical manifestations. Mental retardation was closely correlated with weizure attacks. Neoplasms of the brain, retina, heart, lung and kidneys were all encountered. Hypopigmented macules, intracardiac tumors and infantile spasms were usually the first signs in younger ages and can give hints of earl...
Tuberous Sclerosis: Clinical evaluation of a family and implications for generic counseling: Tuberou...
Objectives: Tuberous sclerosis (TS) is a multisystemic disease with a genetic component. The central...
Aim: This study was planned with the aim of retrospectively reviewing the clinical and laboratory fi...
Objective Tuberous sclerosis complex is an autosomal dominant neurocutaneous disease that presents w...
We aimed to define clinical characteristics and laboratory findings of tuberous sclerosis in 17 pati...
Tuberous sclerosis complex (TSC) is a multisystem, autosomal dominant disorder affecting children an...
Tuberous sclerosis complex (TSC) is a genetic neurocutaneous condition, which affects multiple organ...
Tuberous sclerosis (TS) or Bourneville’s disease is a rare, multisystemic genetic disorder. It invol...
Tuberous sclerosis is a genetic multisystem disorder characterised by widespread hamartomas in sever...
Tuberous sclerosis (TS) is a neurocutaneous disorder, characterized by mental retardation, epilepsy,...
Aims The Tuberous Sclerosis 2000 Study is the first comprehensive longitudinal study of tuberous scl...
Tuberous sclerosis is a genetic multisystem disorder characterized by widespread hamartomas in sever...
<p><strong>Objective</strong> To explore the clinical features of tuberous sclerosis complex (TSC) ...
Tuberous sclerosis is an autosomal dominant condition, but with a varied clinical picture. In the se...
Tuberous Sclerosis: Clinical evaluation of a family and implications for generic counseling: Tuberou...
Objectives: Tuberous sclerosis (TS) is a multisystemic disease with a genetic component. The central...
Aim: This study was planned with the aim of retrospectively reviewing the clinical and laboratory fi...
Objective Tuberous sclerosis complex is an autosomal dominant neurocutaneous disease that presents w...
We aimed to define clinical characteristics and laboratory findings of tuberous sclerosis in 17 pati...
Tuberous sclerosis complex (TSC) is a multisystem, autosomal dominant disorder affecting children an...
Tuberous sclerosis complex (TSC) is a genetic neurocutaneous condition, which affects multiple organ...
Tuberous sclerosis (TS) or Bourneville’s disease is a rare, multisystemic genetic disorder. It invol...
Tuberous sclerosis is a genetic multisystem disorder characterised by widespread hamartomas in sever...
Tuberous sclerosis (TS) is a neurocutaneous disorder, characterized by mental retardation, epilepsy,...
Aims The Tuberous Sclerosis 2000 Study is the first comprehensive longitudinal study of tuberous scl...
Tuberous sclerosis is a genetic multisystem disorder characterized by widespread hamartomas in sever...
<p><strong>Objective</strong> To explore the clinical features of tuberous sclerosis complex (TSC) ...
Tuberous sclerosis is an autosomal dominant condition, but with a varied clinical picture. In the se...
Tuberous Sclerosis: Clinical evaluation of a family and implications for generic counseling: Tuberou...
Objectives: Tuberous sclerosis (TS) is a multisystemic disease with a genetic component. The central...
Aim: This study was planned with the aim of retrospectively reviewing the clinical and laboratory fi...