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Results 1 - 10 of 68 for Cortical
  1. Caffey disease 
    Caffey disease, also called infantile cortical hyperostosis, is a bone disorder that most often occurs in babies. Excessive new bone formation (hyperostosis) is characteristic of Caffey disease. ...
    https://medlineplus.gov/genetics/condition/caffey-disease - Genetics
  2. MTOR gene 
    ... development of the brain. This spectrum includes focal cortical dysplasia, which is characterized by malformation of the outer surface of the brain (the cerebral cortex), and hemimegalencephaly, which is enlargement of one side ...
    https://medlineplus.gov/genetics/gene/mtor - Genetics
  3. Bartter syndrome 
    ... of the condition. Aldosteronism with hyperplasia of the adrenal cortex Bartter disease Bartter's syndrome Juxtaglomerular hyperplasia with ...
    https://medlineplus.gov/genetics/condition/bartter-syndrome - Genetics
  4. Familial hemiplegic migraine 
    Familial hemiplegic migraine is a form of migraine headache that runs in families. Migraines usually cause intense, throbbing pain in one area of the head, often ...
    https://medlineplus.gov/.../condition/familial-hemiplegic-migraine - Genetics
  5. CACNA1A gene 
    The CACNA1A gene belongs to a family of genes that provide instructions for making calcium channels. These channels, which transport positively charged calcium ...
    https://medlineplus.gov/genetics/gene/cacna1a - Genetics
  6. X-linked adrenal hypoplasia congenita 
    X-linked adrenal hypoplasia congenita is a disorder that is noticeable from birth (congenital) and affects the development of the adrenal glands, which ...
    https://medlineplus.gov/.../x-linked-adrenal-hypoplasia-congenita - Genetics
  7. NNT gene 
    The NNT gene provides instructions for making an enzyme called nicotinamide nucleotide transhydrogenase. This enzyme is found embedded in the inner membrane ...
    https://medlineplus.gov/genetics/gene/nnt - Genetics
  8. Fukuyama congenital muscular dystrophy 
    Fukuyama congenital muscular dystrophy is an inherited condition that predominantly affects the muscles, brain, and eyes. Congenital muscular dystrophies are ...
    https://medlineplus.gov/.../fukuyama-congenital-muscular-dystrophy - Genetics
  9. MC2R gene 
    The MC2R gene provides instructions for making a protein called adrenocorticotropic hormone (ACTH) receptor. This protein is found primarily in the adrenal ...
    https://medlineplus.gov/genetics/gene/mc2r - Genetics
  10. Polymicrogyria 
    ... parasagittal parieto-occipital polymicrogyria Genetic Testing Registry: Complex cortical dysplasia with other brain malformations 7 Bilateral frontal ...
    https://medlineplus.gov/genetics/condition/polymicrogyria - Genetics
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