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An Egyption family with H syndrome..

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An Egyptian family with H syndrome due to a novel mutation in SLC29A3 illustrating overlapping features with pigmented hypertrichotic dermatosis with insulin-dependent diabetes and Faisalabad histiocytosis

 

  1. Nancy S Elbarbary1,†,
  2. Erling Tjora2,3,†,
  3. Janne Molnes2,3,
  4. Benedicte A Lie4,
  5. Mohammad A Habib5,
  6. Mona A Salem1 and
  7. Pål Rasmus Njølstad2,3,*

 

Article first published online: 18 SEP 2012

Pediatric Diabetes

Volume 14, Issue 6, pages 466–472, September 2013