Partial Agenesis of Corpus Callosum in Sanjad-Sakati Syndrome (p-ACC)
نویسندگان
چکیده
منابع مشابه
Partial agenesis of corpus callosum in Sanjad-Sakati syndrome (p-ACC).
middleeast in children of consanguineous parents1. it is a rare autosomal recessive disorder known also as middle-east syndrome or Richadson-Kirk syndrome or hypoparathyroidism -retardation-dysmorphism (HRd) syndrome2. Children afflicted with this condition are born with intrauterine growth retardation, and present with hypocalcemic tetany or seizures due to hypoparathyroidism at an early stage...
متن کاملSanjad-Sakati Syndrome in Sudanese children.
We report on the first 4 cases (3 girls and one boy belonging to 4 families) of Sanjad-Sakati syndrome from Sudan. They presented within the first 2 months of life with repeated hypocalcaemic convulsions, severe growth retardation and dysmorphic features. They all had low parathyroid hormone levels. All patients came from consanguineous families who are of Arab descent, and 8 of their siblings ...
متن کاملSanjad-Sakati Syndrome in Omani children.
Sanjad Sakati Syndrome is an Autosomal Recessive disorder found exclusively in people of Arabian origin. It was first reported from the Kingdom of Saudi Arabia in 1988. This is a report of a family with this rare disease in Oman. The syndrome comprises of congenital hypoparathyroidism, severe growth retardation, low IQ and typical facial features. Supportive treatment in the form of vitamin D a...
متن کاملNeurodevelopmental Outcome of Patients With Agenesis of Corpus Callosum
Background: Agenesis of Corpus Callosum (ACC) is a type of brain dysgenesis with various clinical manifestations. Objectives: This study aimed to investigate the clinical and neurodevelopmental outcomes of patients with ACC. Materials & Methods: In this cross-sectional study, the clinical and neurodevelopmental conditions of 62 patients with complete ACC referred to subspecialty clinics of pe...
متن کاملCorpus callosum agenesis.
OBJECTIVE The objectives are to analyse corpus callosum agenesis in children with various neurological problems in a hospital set-up, and to study the neurological and systemic abnormalities associated with this condition. METHODS The children with various neurological problems who underwent computerized tomography brain from January 1993 to December 1997, and were found to have corpus callos...
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ژورنال
عنوان ژورنال: Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques
سال: 2012
ISSN: 0317-1671,2057-0155
DOI: 10.1017/s0317167100015705