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Results 1 - 6 of 6 for "Microcephaly," cortical "malformations," intellectual disability
  1. Isolated lissencephaly sequence 
    ... In people with ILS, the cells of the cerebral cortex are disorganized, and the ... delayed development, and recurrent seizures (epilepsy) in individuals ...
    https://medlineplus.gov/.../isolated-lissencephaly-sequence - Genetics
  2. DYRK1A gene 
    ... speech problems, anxiety, and an unusually small head (microcephaly). Other ... intellectual disability syndrome.DYRK1A gene mutations result in loss of ...
    https://medlineplus.gov/genetics/gene/dyrk1a - Genetics
  3. Periventricular heterotopia 
    ... usually have normal intelligence, although some have mild intellectual disability. ... delays, recurrent infections, blood vessel abnormalities, stomach ...
    https://medlineplus.gov/.../condition/periventricular-heterotopia - Genetics
  4. Autosomal recessive primary microcephaly 
    ... MICROCEPHALY 2, PRIMARY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT CORTICAL MALFORMATIONS; MCPH2 MICROCEPHALY 4, PRIMARY, AUTOSOMAL RECESSIVE; MCPH4 MICROCEPHALY 3, PRIMARY, ...
    https://medlineplus.gov/.../autosomal-recessive-primary-microcephaly - Genetics
  5. Congenital fibrosis of the extraocular muscles 
    ... CFEOM3 can include additional neurological problems, such as intellectual disability; difficulty with social skills; a smaller-than-normal head size (microcephaly); muscle weakness in the face; nonfunctioning vocal cords; ...
    https://medlineplus.gov/...nital-fibrosis-of-the-extraocular-muscles - Genetics
  6. FOXG1 syndrome 
    ... is associated with a particular pattern of brain malformations that includes ... disability. Abnormal or involuntary movements, such as jerking movements ...
    https://medlineplus.gov/genetics/condition/foxg1-syndrome - Genetics