Brain Malformations

Related topics on Genetics Home Reference:

• Aicardi syndrome
• Alström syndrome
• Amish lethal microcephaly
• Andermann syndrome
• anencephaly
• Apert syndrome
• autosomal recessive primary microcephaly
• Baraitser-Winter syndrome
• Beare-Stevenson cutis gyrata syndrome
• Carpenter syndrome
• cerebral cavernous malformation
• Charcot-Marie-Tooth disease
• congenital cataracts, facial dysmorphism, and neuropathy
• congenital insensitivity to pain with anhidrosis
• Crouzonodermoskeletal syndrome
• Dandy-Walker syndrome
• familial dysautonomia
• giant axonal neuropathy
• hereditary neuropathy with liability to pressure palsies
• hereditary sensory and autonomic neuropathy type IE
• hereditary sensory and autonomic neuropathy type II
• hereditary sensory and autonomic neuropathy type V
• hereditary sensory neuropathy type 1
• infantile-onset ascending hereditary spastic paralysis
• Jackson-Weiss syndrome
• L1 syndrome
• Meckel syndrome
• Miller-Dieker syndrome
• Muenke syndrome
• nonsyndromic holoprosencephaly
• Pallister-Hall syndrome
• periventricular heterotopia
• Pfeiffer syndrome
• polymicrogyria
• pontocerebellar hypoplasia
• Refsum disease
• Saethre-Chotzen syndrome
• septo-optic dysplasia
• Shprintzen-Goldberg syndrome
• Silver syndrome
• Smith-Magenis syndrome
• spastic paraplegia type 11
• spastic paraplegia type 2
• spastic paraplegia type 3A
• spastic paraplegia type 4
• spastic paraplegia type 7
• spastic paraplegia type 8
• spina bifida
• trisomy 13
• Troyer syndrome
• tuberous sclerosis complex
• X-linked lissencephaly

You may also search Genetics Home Reference for "Brain Malformations" for additional information.