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Results 1 - 10 of 167 for Child syndrome
  1. CHILD syndrome 
    CHILD syndrome is a condition that affects the development of several parts of the body. The name of the condition is an acronym of the major features: congenital ...
    https://medlineplus.gov/genetics/condition/child-syndrome - Genetics
  2. Surfactant dysfunction 
    Surfactant dysfunction is a lung disorder that causes breathing problems. This condition results from abnormalities in the composition or function of surfactant, ...
    https://medlineplus.gov/genetics/condition/surfactant-dysfunction - Genetics
  3. NSDHL gene 
    ... the NSDHL gene have been found to cause CHILD syndrome, a condition that can affect the development of ... cholesterol synthesis leads to the specific features of CHILD syndrome. More About This Health Condition Variants in the ...
    https://medlineplus.gov/genetics/gene/nsdhl - Genetics
  4. MTR gene 
    ... variant also increases the risk of having a child with Down syndrome, which is a condition characterized by intellectual disability ... homocysteinemia are three risk factors for having a child with Down syndrome. Am J Med Genet A. 2003 Sep 1; ...
    https://medlineplus.gov/genetics/gene/mtr - Genetics
  5. Williams syndrome 
    ... their family. However, the risk of having a child with Williams syndrome is increased if a parent, who is unaffected, ... Bjornstad PG, Ramstad K. Prevalence estimation of Williams syndrome. J Child Neurol. 2002 Apr;17(4):269-71. doi: ...
    https://medlineplus.gov/genetics/condition/williams-syndrome - Genetics
  6. Down syndrome 
    ... Although women of any age can have a child with Down syndrome, the chance of having a child with this condition increases as a woman gets older. Most cases of Down syndrome result from trisomy 21, which means each cell ...
    https://medlineplus.gov/genetics/condition/down-syndrome - Genetics
  7. Klinefelter syndrome 
    ... sperm cell with one Y chromosome, the resulting child will have Klinefelter syndrome. Similarly, if a sperm cell with both an ... cell with a single X chromosome, the resulting child will have Klinefelter syndrome.Mosaic Klinefelter syndrome (46,XY/47,XXY) is ...
    https://medlineplus.gov/genetics/condition/klinefelter-syndrome - Genetics
  8. Ring chromosome 20 syndrome 
    ... 20 being passed from a parent to a child. R(20) syndrome Ring 20 syndrome Ring chromosome 20 Ring chromosome ... H, Gokben S, Ozkinay F. Ring chromosome 20 syndrome with intractable epilepsy. Dev Med Child Neurol. 2005 May;47(5):343-6. doi: ...
    https://medlineplus.gov/.../condition/ring-chromosome-20-syndrome - Genetics
  9. Muenke syndrome 
    ... Tamburrini G, Caldarelli M, Di Rocco C. Muenke syndrome. Childs Nerv Syst. 2004 May;20(5):297-301. doi: 10.1007/s00381-003-0906-y. Epub 2004 Feb 10. Citation on PubMed ... and Crouzon syndrome with acanthosis nigricans. Endocr Rev. 2000 Feb;21( ...
    https://medlineplus.gov/genetics/condition/muenke-syndrome - Genetics
  10. Horner syndrome 
    ... J. Agenesis of internal carotid artery in a child with ipsilateral Horner's syndrome. J Child Neurol. 2009 Jan;24(1):101-4. doi: 10.1177/0883073808321049. Citation on PubMed Jeffery AR, Ellis FJ, Repka MX, Buncic JR. Pediatric Horner syndrome. J AAPOS. 1998 Jun;2(3):159-67. ...
    https://medlineplus.gov/genetics/condition/horner-syndrome - Genetics
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