Dolichol kinase deficiency

Dolichol kinase deficiency is a cutaneous condition caused by a mutation in the dolichol kinase gene.[2][3]

Dolichol kinase deficiency
Other namesHypotonia and ichthyosis due to dolichol phosphate deficiency[1]
This condition is inherited in an autosomal recessive manner.

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

See also

References
  1. RESERVED, INSERM US14-- ALL RIGHTS. "Orphanet: DK1 CDG". www.orpha.net. Retrieved 11 April 2019.
  2. Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. ISBN 978-1-4160-2999-1.
  3. 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. doi:10.1086/512130. PMC 1821118. PMID 17273964.










Classification
External resources


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