Dyskeratosis congenita

Dyskeratosis congenita (DC) is a rare ectodermal dysplasia that often presents with the classic triad of nail dysplasia, skin pigmentary changes, and oral leukoplakia associated with a high risk of bone marrow failure (BMF) and cancer.

Diabetes mellitus

A group of abnormalities characterized by hyperglycemia and glucose intolerance.


Total: 2

                      


(per page)
PMID (PMCID)
1376473
MALE Child
Dyskeratosis congenita associated with elevated fetal hemoglobin, X-linked ocular albinism, and juvenile-onset diabetes mellitus.
Reichel M, Grix AC, Isseroff RR.
Pediatr Dermatol. 1992;9(2):103-6.
An 11-year-old boy had dyskeratosis congenita, elevated fetal hemoglobin level, X-linked ocular albinism, and juvenile-onset diabetes mellitus.
1376473
MALE Child
Dyskeratosis congenita associated with elevated fetal hemoglobin, X-linked ocular albinism, and juvenile-onset diabetes mellitus.
Reichel M, Grix AC, Isseroff RR.
Pediatr Dermatol. 1992;9(2):103-6.
Dyskeratosis congenita associated with elevated fetal hemoglobin, X-linked ocular albinism, and juvenile-onset diabetes mellitus.