Arthrogryposis–Renal Dysfunction–Cholestasis Syndrome

Arthrogryposis–renal dysfunction–cholestasis syndrome
Other names: ARC syndrome[1]
A–D: Person AB. Aged (A) 3 years and (B) 5 years. Hyperkeratosis and lichenification of palm of right hand (C) and sole of left foot (D). E–I: Person CD. Facies aged 3 (E); in plaster after corrective hip surgery (F). Hyperkeratosis, dorsum of right foot (G). Radiographs of right foot showing vertical talus (H) and of pelvis showing hip dislocation (I).
Specialty	Dermatology

Arthrogryposis–renal dysfunction–cholestasis syndrome is a cutaneous condition caused by a mutation in the VPS33B gene.^[2] Most of the cases have been survived for infancy. Recently, College of Medical Sciences in Nepal reports a case of ARC syndrome in a girl at the age of more than 18 years.

See also[edit | edit source]

• Multiple sulfatase deficiency
• List of cutaneous conditions

References[edit | edit source]

External links[edit | edit source]

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