LD28.2
category
Genetically-determined cutis laxa
Also indexed as
ADCL - [Autosomal dominant cutis laxa] (MIM 123700)ARCL-1 - [Autosomal recessive cutis laxa, type 1] (MIM 219100)ARCL-2A - [Autosomal recessive cutis laxa, type 2A] (MIM 219200)ARCL-2B - [Autosomal recessive cutis laxa, type 2B] (MIM 612940)ARCL-3 - [Autosomal recessive cutis laxa, type 3] (MIM 219150)Autosomal dominant cutis laxaAutosomal recessive cutis laxaAutosomal recessive cutis laxa with severe systemic involvementAutosomal recessive cutis laxa, Debré typeAutosomal recessive cutis laxa, pulmonary emphysema typeAutosomal recessive cutis laxa, type 1Autosomal recessive cutis laxa, type 2AAutosomal recessive cutis laxa, type 2BAutosomal recessive cutis laxa, type 3Cutis laxa - Marfanoid syndromeCutis laxa - corneal clouding - intellectual deficitCutis laxa with bone dystrophyCutis laxa with joint laxity and developmental delayCutis laxa with severe pulmonary, gastrointestinal and urinary anomaliesDe Barsy syndromeEhlers-Danlos syndrome type IXGenetically-determined cutis laxaMACS - [Macrocephaly – alopecia – cutis laxa – scoliosis syndrome]MACS syndromeMacrocephaly – alopecia – cutis laxa – scoliosis syndromeOHS - [occipital horn syndrome]Occipital horn syndromeProgeroid syndrome, De Barsy typeSCARF syndromeSkeletal abnormalities – Cutis laxa – craniostenosis – Ambiguous genitalia – psychomotor Retardation and Facial abnormalitiesSyndromic cutis laxaURDS - [Urban-Rifkin-Davis syndrome] (MIM 613177)Urban-Rifkin-Davis syndromeX-linked cutis laxa