Arthrogryposis–renal dysfunction–cholestasis syndrome

Medical condition

Arthrogryposis–renal dysfunction–cholestasis syndrome
Other names	ARC syndrome

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.

References

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.

Classification	D ICD-10: Q89.7 OMIM: 208085 MeSH: C535382
External resources	Orphanet: 2697

Vesicle formation

Lysosome/Melanosome:	HPS1–HPS7 Hermansky–Pudlak syndrome LYST Chédiak–Higashi syndrome
COPII:	SEC23A Cranio-lenticulo-sutural dysplasia
COG7 CDOG IIE
APC:	AP1S2 X-linked intellectual disability AP3B1 Hermansky–Pudlak syndrome 2 AP4M1 CPSQ3

ARL6 BBS3
RAB27A Griscelli syndrome 2
CHM Choroideremia MLPH Griscelli syndrome 3

Myosin:	MYO5A Griscelli syndrome 1
Microtubule:	SPG4 Hereditary spastic paraplegia 4
Kinesin:	KIF5A Hereditary spastic paraplegia 10
Spectrin:	SPTBN2 Spinocerebellar ataxia 5

Synaptic vesicle:	SNAP29 CEDNIK syndrome STX11 Hemophagocytic lymphohistiocytosis 4
Caveolae:	CAV1 Congenital generalized lipodystrophy 3 CAV3 Limb-girdle muscular dystrophy 2B, Long QT syndrome 9
Vacuolar protein sorting:	VPS33B ARC syndrome VPS13B Cohen syndrome
DYSF Distal muscular dystrophy

See also vesicular transport proteins

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