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There is a page named "Kenny-Caffey syndrome" on Wikipedia

  • Learman syndrome
    )
    Acrocallosal syndrome Adams-Oliver syndrome Adenosine kinase deficiency Antley-Bixler syndrome Autosomal dominant Kenny-Caffey syndrome Autosomal recessive...
    18 KB (1,722 words) - 07:10, 15 April 2024
  • Kennerknecht–Sorgo–Oberhoffer syndrome Kennerknecht–Vogel syndrome KennyCaffey syndrome KennyCaffey syndrome, type 1 Keratitis, hereditary Keratoacanthoma familial...
    5 KB (406 words) - 17:26, 14 March 2022
  • Thumbnail for Optic disc drusen
    include: Alagille syndrome, Down syndrome, Kenny-Caffey syndrome, Leber Hereditary Optic Neuropathy and linear nevus sebaceous syndrome. Patients with optic...
    14 KB (1,543 words) - 11:16, 3 December 2023
  • Kearns–Sayre syndrome – Thomas P. Kearns, George Pomeroy Sayre Kennedy's disease – William R. Kennedy Kennedy's syndrome – Robert Foster Kennedy Kenny-Caffey syndrome...
    62 KB (6,514 words) - 00:22, 1 July 2024
  • 6 months, and 25% of those having permanent hypoparathyroidism. Kenny-Caffey Syndrome Autoimmune invasion and destruction is the most common non-surgical...
    16 KB (1,629 words) - 08:59, 3 February 2024
  • Thumbnail for Sanjad–Sakati syndrome
    hypoparathyroidism-retardation-dysmorphism and autosomal recessive Kenny-Caffey syndrome. Nature Genet. 32: 448-452, 2002. Courtens, W., Wuyts, W., Poot...
    6 KB (630 words) - 02:26, 4 March 2024
  • Thumbnail for Family with sequence similarity 111 member a
    variants in this gene have been associated with dominantly inherited Kenny-Caffey syndrome (KCS; MIM 127000) and the more severe osteocraniostenosis (OCS;...
    4 KB (595 words) - 23:40, 2 December 2023
  • Syndromic microphthalmia is a class of rare congenital anomalies characterized by microphthalmia along with other non-ocular malformations. Syndromic...
    13 KB (538 words) - 09:46, 18 March 2024
  • Thumbnail for TBCE
    PMID 9634513. Diaz GA, Khan KT, Gelb BD (1999). "The autosomal recessive Kenny-Caffey syndrome locus maps to chromosome 1q42-q43". Genomics. 54 (1): 13–8. doi:10...
    7 KB (849 words) - 18:31, 11 October 2022
  • Thumbnail for Andrea Superti-Furga
    the TBX15-related Cousin syndrome, the FAM111A-related disorders Kenny-Caffey syndrome and Osteocraniostenosis, the tartrate-resistant acid phosphatase(ACP5)-related...
    24 KB (2,269 words) - 19:14, 19 April 2024
  • Battered child syndrome
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    bones was similar to that occurring after breech extractions. In 1946, John Caffey, the American founder of paediatric radiology, drew attention to the association...
    208 KB (22,777 words) - 13:47, 5 June 2024
  • Cherish the Life of the World: Selected Letters of Margaret Mead. Margaret M. Caffey and Patricia A. Francis, eds. With foreword by Mary Catherine Bateson. New...
    137 KB (14,115 words) - 11:37, 22 June 2024