Autosomal recessive cutis laxa type 2

MONDO:0019573

A spectrum of connective tissue disorders characterized by the association of wrinkled, redundant and sagging inelastic skin with growth and developmental delay, and skeletal anomalies. The spectrum ranges from patients with classic ARCL2 (ARCL, Debre) type) to patients with a milder form of the disease, wrinkled skin syndrome (WSS).

Also known as: ARCL2, cutis laxa with joint laxity and developmental delay

0 clinical trials for this condition and its sub-types, 0 tagged with Autosomal recessive cutis laxa type 2 itself.

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↑ Autosomal recessive disease (994) ↑ Skeletal dysplasia (660) ↑ Developmental anomaly of metabolic origin (383) ↑ Inherited cutis laxa (2) ↑ Inborn disorder of proline metabolism (0)

Sub-types of Autosomal recessive cutis laxa type 2

Autosomal recessive cutis laxa type 2A 0 trials
1 sub-type
- Wrinkly skin syndrome 0 trials
Autosomal recessive cutis laxa type 2B 0 trials
Autosomal recessive cutis laxa type 2C 0 trials
Autosomal recessive cutis laxa type 2D 0 trials

Including sub-types (0) Tagged with Autosomal recessive cutis laxa type 2 (0)

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