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Nume Macrocephaly/megalencephaly Syndrome, Autosomal Recessive
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Boli A-Z Achondroplasia Alacrima, Achalasia, and Mental Retardation Syndrome Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alport Syndrome, X-Linked Al-Raqad Syndrome Androgen Insensitivity Syndrome, Mild Aniridia 1 Anorexia Nervosa 1 Arthrochalasia Ehlers-Danlos Syndrome Astigmatism Ataxia and Polyneuropathy, Adult-Onset Ataxia-Telangiectasia Autism Autism Spectrum Disorder Band Heterotopia Blood Group--Ahonen Canavan Disease Cerebritis Congenital Cytomegalovirus Cytomegalovirus Infection Dandy-Walker Complex Dwarfism Encephalitis Encephalocele Epilepsy Epileptic Encephalopathy, Early Infantile, 15 Epileptic Encephalopathy, Early Infantile, 7 Familial Thoracic Aortic Aneurysm and Dissection Ganglioneuroma Growth Hormone Deficiency Hemimegalencephaly Hemophilia a Hydrocephalus Hypoglycemia Leukodystrophy Lipomatosis Lissencephaly Macrocephaly, Benign Familial Megalencephaly Megalencephaly-Capillary Malformation-Polymicrogyria Syndrome Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus Syndrome 1 Megalencephaly with Dysmyelination Myopathy Myopia Neuronitis Neuropathy Nevus, Epidermal Occipital Encephalocele Periventricular Nodular Heterotopia Polydactyly Polyhydramnios Polyhydramnios, Megalencephaly, and Symptomatic Epilepsy Polymicrogyria Schimmelpenning-Feuerstein-Mims Syndrome Sinusitis Spastic Ataxia Spasticity Sturge-Weber Syndrome Sudden Infant Death Syndrome Tetraamelia Syndrome, Autosomal Recessive Three M Syndrome 1 Tuberous Sclerosis Weber Syndrome