Arthrogryposis–renal dysfunction–cholestasis syndrome
(Redirected from Lutz–Richner–Landolt syndrome)
| Arthrogryposis–renal dysfunction–cholestasis syndrome | |
|---|---|
| Other names | ARC syndrome[1] |
 | |
| Arthrogryposis–renal dysfunction–cholestasis syndrome is inherited in an autosomal recessive manner. | |
| Specialty | Dermatology |
Arthrogryposis–renal dysfunction–cholestasis syndrome is a cutaneous condition caused by a mutation in the VPS33B gene.[2]
See also
[edit]References
[edit]- ^ RESERVED, INSERM US14-- ALL RIGHTS. "Orphanet: Arthrogryposis renal dysfunction cholestasis syndrome". www.orpha.net. Retrieved 18 May 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.