in an Infant Poliosis y estatus epiléptico en un lactante como presentación de esclerosis tuberosa To t he Edit or: Tuberous sclerosis (TS) is a neurocutaneous syndrome with an autosomal dominant pattern of inheritance and a high penetrance. It is characterized by the appearance of hamartomatous lesions in several organs,1 and the most usual clinical signs of this disease are skin lesions, epilepsy, learning difficulties,2 and behavioral disorders. We report the case of a 51-day-old infant, born at term of nonconsanguineous healthy parents after an uncomplicated pregnancy and delivery, who was seen in the pediatric emergency department due to persistent convulsive seizures that had lasted 3 days. Physical examination revealed th
Tuberous sclerosis complex (TSC) is an autosomal-dominant neurocutaneous disorder with multi-organ i...
Tuberous Sclerosis Complex is an autosomal dominant phakomatosis. This neurocutaneous disorder usual...
Aim: This study was planned with the aim of retrospectively reviewing the clinical and laboratory fi...
Tuberous sclerosis is a genetic multisystem disorder characterized by widespread hamartomas in sever...
Introduction. Tuberous sclerosis or Bourneville-Pringle’s disease is a genetic disorder with an auto...
Tuberous sclerosis (TS) is a genetic disorder characterised by the triad of cutaneous lesions, epile...
Objective Tuberous sclerosis complex is an autosomal dominant neurocutaneous disease that presents w...
In tuberous sclerosis complex (TSC) a relationship has been shown between early and refractory seizu...
he AA. present the longitudinal electroclinical and neuroradiological study of 55 children aged betw...
Tuberous sclerosis complex (TSC) is known to cause severe intractable epilepsy and mental retardatio...
We report a case of tuberous sclerosis in a 19 years old teenage patient with generalized tonic-clon...
We aimed to define clinical characteristics and laboratory findings of tuberous sclerosis in 17 pati...
Epilepsy is the most common neurological symptom in tuberous sclerosis complex (TSC), occurring in 7...
Tuberous sclerosis (TS) or Bourneville’s disease is a rare, multisystemic genetic disorder. It invol...
Tuberous Sclerosis Complex (TSC) is a neurocutaneous disorder characterised by hamartoma formation i...
Tuberous sclerosis complex (TSC) is an autosomal-dominant neurocutaneous disorder with multi-organ i...
Tuberous Sclerosis Complex is an autosomal dominant phakomatosis. This neurocutaneous disorder usual...
Aim: This study was planned with the aim of retrospectively reviewing the clinical and laboratory fi...
Tuberous sclerosis is a genetic multisystem disorder characterized by widespread hamartomas in sever...
Introduction. Tuberous sclerosis or Bourneville-Pringle’s disease is a genetic disorder with an auto...
Tuberous sclerosis (TS) is a genetic disorder characterised by the triad of cutaneous lesions, epile...
Objective Tuberous sclerosis complex is an autosomal dominant neurocutaneous disease that presents w...
In tuberous sclerosis complex (TSC) a relationship has been shown between early and refractory seizu...
he AA. present the longitudinal electroclinical and neuroradiological study of 55 children aged betw...
Tuberous sclerosis complex (TSC) is known to cause severe intractable epilepsy and mental retardatio...
We report a case of tuberous sclerosis in a 19 years old teenage patient with generalized tonic-clon...
We aimed to define clinical characteristics and laboratory findings of tuberous sclerosis in 17 pati...
Epilepsy is the most common neurological symptom in tuberous sclerosis complex (TSC), occurring in 7...
Tuberous sclerosis (TS) or Bourneville’s disease is a rare, multisystemic genetic disorder. It invol...
Tuberous Sclerosis Complex (TSC) is a neurocutaneous disorder characterised by hamartoma formation i...
Tuberous sclerosis complex (TSC) is an autosomal-dominant neurocutaneous disorder with multi-organ i...
Tuberous Sclerosis Complex is an autosomal dominant phakomatosis. This neurocutaneous disorder usual...
Aim: This study was planned with the aim of retrospectively reviewing the clinical and laboratory fi...