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Nume Pachygyria
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Boli A-Z Al-Raqad Syndrome Aniridia 1 Anorexia Nervosa 1 Arachnoid Cysts Arachnoiditis Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis Multiplex Congenita, Neurogenic, with Myelin Defect Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Athetosis Band Heterotopia Baraitser-Winter Syndrome Behr Syndrome Blood Group--Ahonen Blood Group, I System Cataract 40 Cataract, Total Congenital Cerebellar Hypoplasia Cerebritis Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction Chromosomal Triplication Chromosome 17p13.3, Centromeric, Duplication Syndrome Cocaine Antenatal Exposure Congenital Cytomegalovirus Congenital Nervous System Abnormality Craniopharyngioma Cutis Laxa Cytomegalovirus Infection Distal Hereditary Motor Neuropathy, Type Ii Duane Retraction Syndrome Dystonia Encephalopathy Epilepsy Epilepsy with Myoclonic Absences Fanconi Anemia, Complementation Group E Goldberg-Shprintzen Syndrome Hydrocephalus Hypoparathyroidism, Sensorineural Deafness, and Renal Disease Hypotonia Lennox-Gastaut Syndrome Leukodystrophy Lissencephaly Lissencephaly 1 Lissencephaly 4 Lissencephaly with Cerebellar Hypoplasia Lissencephaly, X-Linked, 1 Mast Cell Activation Syndrome Microcephaly Microlissencephaly Myopathy Myopia Neuraminidase Deficiency Neuronal Migration Disorders Neuronitis Nipples Inverted Pachygyria, Frontotemporal Periventricular Nodular Heterotopia Polymicrogyria Retinitis Subcortical Band Heterotopia Suppressor of Tumorigenicity 3 Tuberous Sclerosis Tubulin, Beta Tubulinopathy-Associated Dysgyria Weaver Syndrome Wrinkles