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Ichthyosis prematurity syndrome information


Ichthyosis prematurity syndrome
SpecialtyDermatology

Ichthyosis prematurity syndrome (IPS) is a dermatological disease with known genetic causes. This syndrome is a rare subcategory of autosomal recessive congenital ichthyosis (ARCI).[1] It is associated with complications in the mid-trimester of a pregnancy leading to premature births.[2] Although most prevalent in individuals of Scandinavian origin, there have also been scattered cases in people of Japanese, Italian and Indian ethnicity.[1][3][4] This disorder is also referred to as ichthyosis congenital type IV.[1]

  1. ^ a b c Klar, J; Gedde-Dahl, T; Larsson, M; et al. (2004). "Assignment of the locus for ichthyosis prematurity syndrome to chromosome 9q33.3-34.13". J Med Genet. 41 (3): 208–212. doi:10.1136/jmg.2003.012567. PMC 1735696. PMID 14985385.
  2. ^ "Ichthyosis Prematurity Syndrome". OMIM. Retrieved 3 December 2015.
  3. ^ Ikuya, Tsuge; Masashi, Morishita; Takema, Kato; et al. (2015). "Identification of novel FATP4 mutations in a Japanese patient with ichthyosis prematurity syndrome". Human Genome Variation. 2: 15003. doi:10.1038/hgv.2015.3. PMC 4785586. PMID 27081519.
  4. ^ Renu, George (2014). "Ichthyosis prematurity syndrome: A case report from India". Journal of the American Academy of Dermatology. 70 (5): AB145. doi:10.1016/j.jaad.2014.01.603. Retrieved 16 October 2015.

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