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Results 41 - 50 of 168 for Child syndrome
  1. Cyclic vomiting syndrome 
    ... Boles RG, Powers AL, Adams K. Cyclic vomiting syndrome plus. J Child Neurol. 2006 Mar;21(3):182-8. doi: 10.2310/7010.2006.00040. Citation on PubMed Boles RG, Zaki EA, ... syndrome (CVS) biologically different conditions? Relationship of adult-onset ...
    https://medlineplus.gov/genetics/condition/cyclic-vomiting-syndrome - Genetics
  2. Cardiofaciocutaneous syndrome 
    ... Rauen KA. Neurological complications of cardio-facio-cutaneous syndrome. Dev Med Child Neurol. 2007 Dec;49(12):894-9. doi: 10.1111/j.1469-8749.2007.00894.x. Citation on PubMed Zenker M. Clinical manifestations of mutations ... Citation on PubMed
    https://medlineplus.gov/.../condition/cardiofaciocutaneous-syndrome - Genetics
  3. Trichohepatoenteric syndrome 
    ... Syndromic (phenotypic) diarrhoea of infancy/tricho-hepato-enteric syndrome. Arch Dis Child. 2014 Jan;99(1):35-8. doi: 10.1136/archdischild-2013-304016. Epub 2013 Oct 9. Citation on PubMed ... diarrhea, or trichohepatoenteric syndrome. Am J Hum Genet. 2012 Apr 6;90( ...
    https://medlineplus.gov/.../condition/trichohepatoenteric-syndrome - Genetics
  4. 17q12 deletion syndrome 
    ... the phenotype of patients with a 17q12 microdeletion syndrome. Arch Dis Child. 2015 Mar;100(3):259-64. doi: 10. ...
    https://medlineplus.gov/genetics/condition/17q12-deletion-syndrome - Genetics
  5. Costeff syndrome 
    ... in the Iraqi-Jewish 'optic atrophy plus' (Costeff) syndrome. Dev Med Child Neurol. 1994 Feb;36(2):167-72. doi: ...
    https://medlineplus.gov/genetics/condition/costeff-syndrome - Genetics
  6. Pitt-Hopkins syndrome 
    ... RC. Development, cognition, and behaviour in Pitt-Hopkins syndrome. Dev Med Child Neurol. 2012 Oct;54(10):925-31. doi: ...
    https://medlineplus.gov/genetics/condition/pitt-hopkins-syndrome - Genetics
  7. HNF1B gene 
    ... the phenotype of patients with a 17q12 microdeletion syndrome. Arch Dis Child. 2015 Mar;100(3):259-64. doi: 10. ...
    https://medlineplus.gov/genetics/gene/hnf1b - Genetics
  8. SLC52A3 gene 
    ... Houlden H, Riphagen S, Lin JP, Raymond FL, Childs AM, Sheridan E, Edwards S, Josifova DJ. Brown-Vialetto-Van Laere syndrome, a ponto-bulbar palsy with deafness, is caused ...
    https://medlineplus.gov/genetics/gene/slc52a3 - Genetics
  9. Riboflavin transporter deficiency neuronopathy 
    ... Houlden H, Riphagen S, Lin JP, Raymond FL, Childs AM, Sheridan E, Edwards S, Josifova DJ. Brown-Vialetto-Van Laere syndrome, a ponto-bulbar palsy with deafness, is caused ...
    https://medlineplus.gov/...lavin-transporter-deficiency-neuronopathy - Genetics
  10. Shwachman-Diamond syndrome 
    ... Hall GW, Dale P, Dodge JA. Shwachman-Diamond syndrome: UK perspective. Arch Dis Child. 2006 Jun;91(6):521-4. doi: 10.1136/adc.2003.046151. Citation on PubMed or Free article on PubMed Central ... syndrome: update from the North American Shwachman-Diamond Syndrome ...
    https://medlineplus.gov/.../condition/shwachman-diamond-syndrome - Genetics
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