Dolichol kinase deficiency

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Dolichol kinase deficiency
Classification and external resources
ICD-10 E77.8
OMIM 610768
Orphanet 91131

Dolichol kinase deficiency is a cutaneous condition caused by a mutation in the dolichol kinase gene.[1][2]

It is also known as Congenital disorder of glycosylation 1m.

See also[edit]


  1. ^ Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. ISBN 1-4160-2999-0. 
  2. ^ Kranz C, Jungeblut C, Denecke J, et al. (March 2007). "A defect in dolichol phosphate biosynthesis causes a new inherited disorder with death in early infancy". Am. J. Hum. Genet. 80 (3): 433–40. PMC 1821118Freely accessible. PMID 17273964. doi:10.1086/512130.