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Results 1 - 7 of 7 for Neurodevelopmental disorder with or without anomalies of the "brain," "eye," or heart
  1. Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart 
    Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart (NEDBEH) is a neurological disorder that can also affect many other body systems. This ...
    https://medlineplus.gov/...thout-anomalies-of-the-brain-eye-or-heart - Genetics
  2. RERE gene 
    ... have been found to cause a condition called neurodevelopmental disorder with or without anomalies of the brain, eye, or heart (NEDBEH). This condition primarily affects brain development, causing ...
    https://medlineplus.gov/genetics/gene/rere - Genetics
  3. Vici syndrome 
    Vici syndrome is a severe disorder that ... characteristic feature of Vici syndrome is a brain abnormality called agenesis of ...
    https://medlineplus.gov/genetics/condition/vici-syndrome - Genetics
  4. PACS1 syndrome 
    ... folds and grooves than normal (described as "simple"). Abnormalities of other ... swallow without chewing. These food issues tend to persist throughout ...
    https://medlineplus.gov/genetics/condition/pacs1-syndrome - Genetics
  5. CUL3-related neurodevelopmental disorder 
    ... away after childhood. Rarely, recurrent seizures (epilepsy), congenital heart abnormalities, or genitourinary abnormalities occur in people with CUL3-related neurodevelopmental disorder. CUL3-related neurodevelopmental disorder is a rare disorder, ...
    https://medlineplus.gov/.../cul3-related-neurodevelopmental-disorder - Genetics
  6. Cerebro-facio-thoracic dysplasia 
    ... facio-thoracic dysplasia, such as abnormalities involving the eyes, skin, or hair. Heart defects, ... Cerebro-facio-thoracic dysplasia ...
    https://medlineplus.gov/.../cerebro-facio-thoracic-dysplasia - Genetics
  7. MN1 C-terminal truncation syndrome 
    ... of the two sides of the cerebellum. These brain abnormalities likely contribute to the ... is thought to be a rare disorder. At least 25 affected individuals have been described ...
    https://medlineplus.gov/.../mn1-c-terminal-truncation-syndrome - Genetics