LD2B
category
Syndromes with premature ageing appearance as a major feature
Definition
A heterogeneous group of hereditary syndromes in which affected individuals do or appear to age at an accelerated rate.
Inclusions
- Cockayne syndrome
- Kindler syndrome
- Progeria
- Progeroid syndromes
- Rothmund-Thomson syndrome
Exclusions
- Cutis laxa
(EE41.0) - Xeroderma pigmentosum
(LD27.1)
Also indexed as
AcrogeriaAtypical Werner syndromeBullous acrokeratotic poikiloderma of Kindler and WearyCOFS - [Cerebro-oculo-facio-skeletal syndrome]COFS - [Cerebrooculofacioskeletal syndrome]Cerebro-oculo-facio-skeletal syndromeCerebrooculofacioskeletal syndromeCockayne syndromeCockayne syndrome type 1Cockayne syndrome type 2Cockayne syndrome type 3Congenital poikiloderma with bullae and progressive cutaneous atrophyGeroderma osteodysplasticumGilford-Hutchinson syndromeGottron syndromeHallermann-Streiff-François syndromeHereditary acrokeratotic poikilodermaHutchinson-Gilford syndromeKindler syndromeMetageriaMulvihill-Smith progeroid syndromeNeonatal progeroid syndromePangeriaPena-Shokeir syndrome type 2Poikiloderma congenitalePoikiloderma of Rothmund-ThomsonProgeriaProgeroid syndromesRothmund-Thomson syndromeRothmund-Thomson syndrome type 1Rothmund-Thomson syndrome type 2Syndromes with premature ageing appearance as a major featureWeary–Kindler syndromeWerner syndromeWiedemann-Rautenstrauch progeroid syndromeWrinkly skin syndromeXeroderma pigmentosum-Cockayne syndrome complexpremature aging syndromeprogeria syndrome
Nearby in Multiple developmental anomalies or syndromes
LD20Syndromes with central nervous system anomalies as a major featureLD21Syndromes with eye anomalies as a major featureLD22Syndromes with dental anomalies as a major featureLD23Syndromes with vascular anomalies as a major featureLD24Syndromes with skeletal anomalies as a major featureLD25Syndromes with face or limb anomalies as a major featureLD26Syndromes with limb anomalies as a major featureLD27Syndromes with skin or mucosal anomalies as a major feature