LD2B
Syndromes with premature ageing appearance as a major feature
Síndromes com aparência de envelhecimento prematuro como uma característica importante
CategoryDefinition
A heterogeneous group of hereditary syndromes in which affected individuals do or appear to age at an accelerated rate.
Exclusions
- Xeroderma pigmentosum
- Cutis laxa
Inclusions
- Progeroid syndromes
- Cockayne syndrome
- Rothmund-Thomson syndrome
- Progeria
- Kindler syndrome
Index Terms
Syndromes with premature ageing appearance as a major featureProgeroid syndromespremature aging syndromeprogeria syndromeCockayne syndromeCockayne syndrome type 1Cockayne syndrome type 2Cockayne syndrome type 3Xeroderma pigmentosum-Cockayne syndrome complexCerebro-oculo-facio-skeletal syndromePena-Shokeir syndrome type 2Cerebrooculofacioskeletal syndromeCOFS - [Cerebro-oculo-facio-skeletal syndrome]COFS - [Cerebrooculofacioskeletal syndrome]Rothmund-Thomson syndromePoikiloderma of Rothmund-ThomsonPoikiloderma congenitaleRothmund-Thomson syndrome type 1Rothmund-Thomson syndrome type 2ProgeriaHutchinson-Gilford syndromeGilford-Hutchinson syndromeWerner syndromePangeriaAtypical Werner syndromeAcrogeriaGottron syndromeWiedemann-Rautenstrauch progeroid syndromeNeonatal progeroid syndromeMulvihill-Smith progeroid syndromeGeroderma osteodysplasticumWrinkly skin syndromeMetageriaHallermann-Streiff-François syndromeKindler syndromeBullous acrokeratotic poikiloderma of Kindler and WearyCongenital poikiloderma with bullae and progressive cutaneous atrophyHereditary acrokeratotic poikilodermaWeary–Kindler syndrome (MIM 173650)