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Results 1 - 10 of 30 for Speech disorder
  1. ... the FOXP2 gene can result in FOXP2-related speech and language disorder, a condition that affects the development of speech ... the FOXP2 gene itself. Less commonly, FOXP2-related speech and language disorder results from a rearrangement of the structure of ...
  2. ... Abnormalities in certain brain regions likely underlie the speech, intellectual, and behavioral problems that can occur in SETBP1 disorder. More About This Health Condition Mutations in the ...
  3. ... disease, a disorder characterized by intellectual disability, impaired speech and movement, and a weakened heart muscle (cardiomyopathy). This disorder affects males more frequently and severely than females; ...
  4. ... neurological disorder characterized by intellectual disability and delayed speech development. A variety of other signs and symptoms can also occur in this disorder, such as weak muscle tone, growth impairment, and ...
  5. ... characterized by intellectual disability and delayed development of speech and motor skills. Other neurological problems that commonly occur in this disorder include seizures, weak muscle tone (hypotonia), movement disorders, ...
  6. ... Individuals with this condition can also experience delayed speech, language or motor skills. Some affected individuals have heart problems separate from long QT syndrome. The severity of CACNA1C-related disorder varies greatly; some people with the condition are ...
  7. ... of polymicrogyria called bilateral frontoparietal polymicrogyria (BFPP). This disorder causes intellectual disability, delayed development, problems with speech and movement, and recurrent seizures (epilepsy). Most of ...
  8. ... individuals often have intellectual disability, developmental delay, ... disorder, a developmental condition that affects communication and social ...
  9. ... others in a socially appropriate manner. Changes in speech and language can also occur, such as problems using the correct word and difficulty with language comprehension. The DCTN1 gene mutation associated with this disorder replaces the amino acid arginine with the amino ...
  10. ... Abnormalities in these brain regions underlie the movement, speech, and learning problems that can occur in TUBB4A-related leukodystrophy. It is unclear what causes the wide range of severity in this disorder. More About This Health Condition At least two ...
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