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Results 1 - 4 of 4 for Cutis "laxa," autosomal dominant 3
  1. Cutis laxa 
    ... RECESSIVE, TYPE IIA; ARCL2A OCCIPITAL HORN SYNDROME; OHS CUTIS LAXA, AUTOSOMAL DOMINANT 3; ADCL3 CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IC; ARCL1C CUTIS LAXA, ...
    https://medlineplus.gov/genetics/condition/cutis-laxa - Genetics
  2. ALDH18A1 gene 
    ... can cause two different types of cutis laxa: autosomal dominant cutis laxa type 3 (ADCL3) and autosomal recessive cutis laxa type 3A (ARCL3A, which is ... 5-Carboxylate Synthase Cause a Progeroid Form of Autosomal-Dominant Cutis Laxa. Am J Hum Genet. 2015 Sep 3;97(3):483-92. doi: 10.1016/j. ...
    https://medlineplus.gov/genetics/gene/aldh18a1 - Genetics
  3. ELN gene 
    ... 81. doi: 10.1016/s1050-1738(03)00065-3. Citation on PubMed ... of autosomal-dominant cutis laxa with report of five ELN mutations. Hum Mutat. ...
    https://medlineplus.gov/genetics/gene/eln - Genetics
  4. Lattice corneal dystrophy type II 
    ... the scalp and forehead, and a condition called cutis laxa, which is characterized by loose skin that lacks ... II. GSN This condition is inherited in an autosomal dominant pattern, which means one copy of the altered ...
    https://medlineplus.gov/.../lattice-corneal-dystrophy-type-ii - Genetics