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Results 71 - 80 of 168 for Child syndrome
  1. FOXC2 gene 
    ... Brice G, Mansour S, Bell R, Collin JR, Child AH, Brady AF, Sarfarazi M, Burnand KG, Jeffery S, Mortimer P, Murday VA. Analysis of the phenotypic abnormalities in lymphoedema-distichiasis syndrome in 74 patients with FOXC2 mutations or linkage ...
    https://medlineplus.gov/genetics/gene/foxc2 - Genetics
  2. Raynaud phenomenon 
    ... with a first-degree relative (parent, sibling or child) who has primary Raynaud phenomenon also have the condition. Raynaud disease Raynaud's Raynaud's disease Raynaud's phenomenon Raynaud's syndrome National Organization for Rare Disorders (NORD) ClinicalTrials.gov ...
    https://medlineplus.gov/genetics/condition/raynaud-phenomenon - Genetics
  3. Floating-Harbor syndrome 
    ... child may have bones more typical of a child of 2. However, bone age is usually normal by age 6 to 12.Delay in speech development (expressive language delay) may be severe in Floating-Harbor syndrome, and language impairment can lead to problems in ...
    https://medlineplus.gov/genetics/condition/floating-harbor-syndrome - Genetics
  4. Chromosome 5 
    ... PubMed Cornish K, Bramble D. Cri du chat syndrome: genotype-phenotype correlations and recommendations for clinical management. Dev Med Child Neurol. 2002 Jul;44(7):494-7. doi: ...
    https://medlineplus.gov/genetics/chromosome/5 - Genetics
  5. Bannayan-Riley-Ruvalcaba syndrome 
    ... SA, McMenamin J, Webb D. Bannayan-Riley-Ruvalcaba syndrome: a cause of extreme macrocephaly and neurodevelopmental delay. Arch Dis Child. 2009 Jul;94(7):553-4. doi: 10. ...
    https://medlineplus.gov/.../bannayan-riley-ruvalcaba-syndrome - Genetics
  6. FBN1 gene 
    ... Comeglio P, Boileau C, Faivre L, Charteris D, Child AH, Arno G. The revised ghent ... G, Boileau C. Marfan syndrome in the third Millennium. Eur J Hum Genet. ...
    https://medlineplus.gov/genetics/gene/fbn1 - Genetics
  7. 49,XXXXY syndrome 
    ... Y chromosome fertilizes this egg cell, the resulting child will have four X chromosomes and one Y chromosome (49,XXXXY) in each of the body's cells. 49,XXXXY chromosomal anomaly Chromosome XXXXY syndrome XXXXY aneuploidy XXXXY syndrome Genetic Testing Registry: 49, ...
    https://medlineplus.gov/genetics/condition/49xxxxy-syndrome - Genetics
  8. Swyer syndrome 
    ... the medical term “dysgenesis” means "abnormal development."Swyer syndrome may be identified before birth, at birth, or later when a child does not go through puberty as usual. Because ...
    https://medlineplus.gov/genetics/condition/swyer-syndrome - Genetics
  9. Kabuki syndrome 
    ... A, Dotta A, Digilio MC, Dallapiccola B. Kabuki syndrome: clinical and molecular diagnosis in the first year of life. Arch Dis Child. 2015 Feb;100(2):158-64. doi: 10. ...
    https://medlineplus.gov/genetics/condition/kabuki-syndrome - Genetics
  10. Alcohol use disorder 
    ... women can cause birth defects and fetal alcohol syndrome, which can lead to lifelong physical and behavioral problems in the affected child. Alcohol use disorder is a very common condition. ...
    https://medlineplus.gov/genetics/condition/alcohol-use-disorder - Genetics
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