Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies

Orpha code: 221145OMIM code: 613177

Definition

A rare, genetic, dermis elastic tissue disorder characterized by generalized cutis laxa associated with severe, usually early-onset, pulmonary emphysema, frequent and severe gastrointestinal and genitourinary involvement (i.e. bladder/intestine diverticula and/or tortuosity, gastrointestinal fragility, hydronephrosis), and mild cardiovascular involvement (typically limited to peripheral pulmonary artery stenosis only).

Disease data
Classification

Malformation syndrome

Synonyms
ARCL1C
Zespół Urbana, Rifkina i Davisa
Autosomal recessive cutis laxa type 1C
Urban-Rifkin-Davis syndrome
ORPHA code
221145
OMIM code
613177
ICD10 code
Q82.8
ICD11 code
LD28.2

No additional description.

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