Autosomal dominant multiple pterygium syndrome
(Redirected from Bartsocas–Papas syndrome)
| Autosomal dominant multiple pterygium syndrome | |
|---|---|
| Other names | Distal arthrogryposis type 8[1] |
 | |
| Autosomal dominant multiple pterygium syndrome is inherited in an autosomal dominant fashion. | |
| Specialty | Dermatology |
Autosomal dominant multiple pterygium syndrome is a cutaneous condition inherited in an autosomal dominant fashion.[2]
Society
[edit]Musician Patrick Henry Hughes has a type of this condition.[3]
See also
[edit]References
[edit]- ^ RESERVED, INSERM US14-- ALL RIGHTS. "Orphanet: Autosomal dominant multiple pterygium syndrome". www.orpha.net. Retrieved 28 September 2019.
{{cite web}}: CS1 maint: numeric names: authors list (link) - ^ Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. ISBN 978-1-4160-2999-1.
- ^ "Louisville Magazine". Archived from the original on 2019-04-25. Retrieved 2019-02-05.