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1,349 Possible Causes for Agenesis of Corpus Callosum, Failure to Thrive, Seizure

  • Lissencephaly

    Symptoms of the disorder may include unusual facial appearance, difficulty swallowing, failure to thrive, muscle spasms, seizures, and severe psychomotor retardation.[] It is to consider lissencephaly in the diagnosis of developmental delay with seizure disorder as many patients may be diagnosed as cerebral palsy.[] MRI showed diffuse pachygyria, moderate thickening of the cortex, enlarged ventricles, agenesis of the corpus callosum and septum pellucidum.[]

  • Septo-Optic Dysplasia

    Marshall-Smith syndrome is characterized by advanced bone age, failure to thrive, respiratory problems, dysmorphic facial features, and variable mental retardation.[] A 7-year-old boy was admitted for a general tonic-clonic seizure with severe hypoglycaemia (1.39 mmol/l).[] An uncommon association of infantile spasms, septo-optic dysplasia, partial agenesis of the corpus callosum and an interhemispheric cyst is described in a child.[]

  • Wolf-Hirschhorn Syndrome

    Accordingly, prenatal-onset growth retardation and failure to thrive have been found to result from haploinsufficiency for a 4p gene located between 0.4 and 1.3 Mb, whereas[] , seizure types, early age of onset, EEG pattern, and responses to specific anti-epileptic drugs.[] […] of the corpus callosum, bilateral renal hypoplasia, and two atrial septal defects.[]

  • Sanjad-Sakati Syndrome

    We encountered a 2-year-old boy with hypocalcemia, failure to thrive and macrocytic anemia.[] Sanjad-Sakati syndrome Other names Hypoparathyroidism-short stature-intellectual disability-seizures syndrome Sanjad-Sakati syndrome is inherited in an autosomal recessive[] Partial Agenesis of Corpus Callosum in Sanjad-Sakati Syndrome (p-ACC) To send this article to your Dropbox account, please select one or more formats and confirm that you[]

  • Mowat-Wilson Syndrome

    Symptons may include: Growth and Motor development delay : speech can be delayed or absent; Seizures in the majority of individuals ( Epilepsy ); Failure to thrive in early[] Fever-induced seizures can be presenting signs of MWS.[] […] of the corpus callosum.[]

  • Methylmalonic Acidemia

    Cranial MRI scans showed bilateral cerebral atrophy (n 14), increased T2 signal intensities in white matter (n 12), agenesis of corpus callosum (n 2), bilateral increased[] See a provider if your child has signs of failure-to-thrive or developmental delays. A low-protein diet can help reduce the number of acidemia attacks.[] At 9 months of age, he developed brief tonic seizures, which showed polyspike bursts under EEG. His psychomotor development continued to deteriorate.[]

  • Autosomal Recessive Primary Microcephaly Type 10

    […] of the corpus callosum Hypermetropia Lissencephaly Heterotopia Pachygyria Sloping forehead Polymicrogyria Agenesis of corpus callosum Abnormal facial shape Coarctation of[] PCH3 ( OMIM ) is characterized by hypotonia, hyperreflexia, microcephaly, optic atrophy, and seizures.[] Of The Corpus Callosum With Peripheral Neuropathy ... ...[]

  • Fetal Warfarin Syndrome

    Associated conditions include hypoplasia of nasal bridge, laryngomalacia, pectus carinatum, congenital heart defects, ventriculomegaly, agenesis of the corpus callosum, stippled[] Blindness, deafness, and seizures, as well as severe bleeding at birth, not predictable from the maternal international normalized ratio, may also be seen.[] […] of corpus callosum microcephaly microphthalmia congenital cataracts cardiovascular congenital cardiac anomalies Warfarin is a teratogenic drug.[]

  • Leigh's Disease

    In the other case, there was an agenesis of the corpus callosum, the second instance in which a malformation of the corpus callosum was associated with this condition.[] Constitutional symptoms, such as malaise, fatigue, anorexia and failure to thrive are present in many patients, while respiratory and gastrointestinal disturbances such as[] Symptoms usually begin between ages of three months and two years and include loss of appetite, vomiting, irritability and seizure activity.[]

  • Emanuel Syndrome

    Affiliated tissues include heart , kidney and skin , and related phenotypes are low-set ears and agenesis of corpus callosum Genetics Home Reference : 25 Emanuel syndrome[] The disorder involves a wide range of abnormalities such as kidney, genital and heart abnormalities, mental retardation, small head and failure to thrive.[] In addition, patients with Emanuel syndrome may have seizure disorders.[]

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