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Results 1 - 6 of 6 for child health human development
  1. Swyer syndrome 
    ... RM, Vilain E. Translational genetics for diagnosis of human disorders of sex development. Annu Rev Genomics Hum Genet. 2013;14:371- ... EC, Vilain E. Towards improved genetic diagnosis of human differences of sex development. Nat Rev Genet. 2021 Sep;22(9):588- ...
    https://medlineplus.gov/genetics/condition/swyer-syndrome - Genetics
  2. Williams syndrome 
    ... AP, Maconochie M, Donnai D. GTF2IRD1 in craniofacial development of humans and mice. Science. 2005 Nov 18;310(5751): ...
    https://medlineplus.gov/genetics/condition/williams-syndrome - Genetics
  3. Isolated congenital asplenia 
    ... infections in children with asplenia or hyposplenia. Paediatr Child Health. 2014 May;19(5):271-8. Citation on ...
    https://medlineplus.gov/.../condition/isolated-congenital-asplenia - Genetics
  4. Heterotaxy syndrome 
    ... H, Xia H, Deng S. Genetic basis of human left-right asymmetry disorders. Expert Rev Mol Med. ...
    https://medlineplus.gov/genetics/condition/heterotaxy-syndrome - Genetics
  5. Kabuki syndrome 
    ... fetal finger pads because they normally occur in human fetuses; in most people they disappear before birth. ... to activate certain genes that are important for development.Between 2 and 6 percent of cases of ...
    https://medlineplus.gov/genetics/condition/kabuki-syndrome - Genetics
  6. Acute necrotizing encephalopathy type 1 
    ... that are known to trigger this condition include human herpesvirus 6, coxsackie virus, and enteroviruses. In rare ... the signs and symptoms of this condition. The health history of the individual, such as nutritional status and ... CM, Schelling DK, Eiben RM, Kerr DS, Anderson J, Bassuk AG, Bye AM, Childs AM, Clarke A, Crow YJ, Di Rocco M, ...
    https://medlineplus.gov/.../acute-necrotizing-encephalopathy-type-1 - Genetics