Results 1 - 4 of 4 for Cutis "laxa," autosomal dominant
  1. Rare Diseases and Related Terms From the National Institutes of Health (Office of Rare Diseases)  
    ... narcolepsy * ADCAII - See Spinocerebellar ataxia 7 * ADCL - See Cutis laxa, autosomal dominant * Addison disease - See Addison's disease * Addison-Biermer anemia - ... ophthalmic outburst syndrome * Autosomal dominant cutis laxa - See Cutis laxa, autosomal ... Autosomal dominant deafness-onychodystrophy syndrome - See Autosomal dominant ...
  2. Genetics Home Reference: Cutis laxa From the National Institutes of Health (National Library of Medicine)  
    ... recessive cutis laxa type IA Genetic Testing Registry: Cutis laxa, autosomal dominant Genetic Testing Registry: Cutis laxa, X-linked Genetic ... Health Professionals What glossary definitions help with understanding cutis laxa? aneurysm ; ... calcium ; cell ; chromosome ; congenital ; connective tissue ; ...
  3. Heritable Disorders of Connective Tissue From the National Institutes of Health (National Institute of Arthritis and Musculoskeletal and Skin Diseases)  
    ... Cutis laxa. Latin for loose or lax skin, cutis laxa refers to an extremely rare ... Dominant. A genetic trait (or genetically transmitted disorder) that ...
  4. ... the scalp and forehead, and a condition called cutis laxa, which is characterized by loose skin that lacks ... facial expression that appears sad. Read more about cutis laxa . How common is lattice corneal dystrophy type II? ...
Refine by Type
  • All Results (4)
  • Health Topics
  •  External Health Links (4)
  • Drugs and Supplements
  • Medical Encyclopedia
  • Videos and Tutorials
  • News
  • MedlinePlus Magazine
  • Other Resources
  • Multiple Languages