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Results 61 - 70 of 92 for Speech delay
  1. Troyer syndrome 
    ... over time. Common features of Troyer syndrome include delays in learning to walk and ... (dysarthria), skeletal (bone) abnormalities, and mood swings. ...
    https://medlineplus.gov/genetics/condition/troyer-syndrome - Genetics
  2. PURA gene 
    ... characterized by severely delayed or impaired development of speech and walking, ... delay, hypotonia, and other neurological problems in people with ...
    https://medlineplus.gov/genetics/gene/pura - Genetics
  3. MN1 gene 
    ... gene have been associated with hearing loss and speech problems without other ... disabilities, and craniofacial abnormalities. While these features ...
    https://medlineplus.gov/genetics/gene/mn1 - Genetics
  4. TRNT1 deficiency 
    ... deficiency. Many affected individuals have delayed development of speech and motor ... delay (SIFD) and a milder disorder called retinitis pigmentosa ...
    https://medlineplus.gov/genetics/condition/trnt1-deficiency - Genetics
  5. SETBP1 haploinsufficiency disorder 
    ... Abnormalities in certain brain regions likely underlie the speech, intellectual, and behavioral problems that ... Genetic ...
    https://medlineplus.gov/.../setbp1-haploinsufficiency-disorder - Genetics
  6. 1q21.1 microduplication 
    ... people with a 1q21.1 microduplication have developmental delay and ... of speech and language. Expressive language skills (vocabulary and the ...
    https://medlineplus.gov/genetics/condition/1q211-microduplication - Genetics
  7. Microcephaly, seizures, and developmental delay 
    Microcephaly, seizures, and ... speak. Intellectual disability and behavior problems, primarily hyperactivity, are ...
    https://medlineplus.gov/...ocephaly-seizures-and-developmental-delay - Genetics
  8. Farber lipogranulomatosis 
    ... multiple body systems. Affected individuals can have developmental delay, ... of speech, or involuntary muscle jerks (myoclonus). People with Farber ...
    https://medlineplus.gov/genetics/condition/farber-lipogranulomatosis - Genetics
  9. PURA syndrome 
    ... in PURA are associated with hypotonia and developmental delay. Cold Spring Harb Mol ... or Free article on PubMed Central
    https://medlineplus.gov/genetics/condition/pura-syndrome - Genetics
  10. Biotin-thiamine-responsive basal ganglia disease 
    ... ophthalmoplegia), difficulty chewing or swallowing (dysphagia), and slurred ... disorders, and delay in the development of mental and motor skills ( ...
    https://medlineplus.gov/...thiamine-responsive-basal-ganglia-disease - Genetics
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