LD2B

早衰综合征

Syndromes with premature ageing appearance as a major feature

类目第 20 章发育异常

上级条目: 多发性发育异常或综合征
层级: 3 级

定义

一组异质性遗传综合征，其中受影响的个体确实或似乎正在加速衰老。

A heterogeneous group of hereditary syndromes in which affected individuals do or appear to age at an accelerated rate.

包含词该编码包含的临床情况，通常不作为独立编码

早衰综合征
Cockayne综合征
Rothmund-Thomson综合征
早老症
Kindler综合征

英文词条（5）

Progeroid syndromes
Cockayne syndrome
Rothmund-Thomson syndrome
Progeria
Kindler syndrome

除外词明确排除、需编到其他条目的情况

英文词条（2）

跨章引用同一概念在其他章节另有编码

英文词条（5）

索引词可用于检索该条目的同义词与别名

英文词条（39）

Syndromes with premature ageing appearance as a major feature
Progeroid syndromes
premature aging syndrome
progeria syndrome
Cockayne syndrome
Cockayne syndrome type 1
Cockayne syndrome type 2
Cockayne syndrome type 3
Xeroderma pigmentosum-Cockayne syndrome complex
Cerebro-oculo-facio-skeletal syndrome
COFS - [Cerebro-oculo-facio-skeletal syndrome]
COFS - [Cerebrooculofacioskeletal syndrome]
Cerebrooculofacioskeletal syndrome
Pena-Shokeir syndrome type 2
Rothmund-Thomson syndrome
Poikiloderma congenitale
Poikiloderma of Rothmund-Thomson
Rothmund-Thomson syndrome type 1
Rothmund-Thomson syndrome type 2
Progeria
Gilford-Hutchinson syndrome
Hutchinson-Gilford syndrome
Werner syndrome
Pangeria
Atypical Werner syndrome
Acrogeria
Gottron syndrome
Wiedemann-Rautenstrauch progeroid syndrome
Neonatal progeroid syndrome
Mulvihill-Smith progeroid syndrome
Geroderma osteodysplasticum
Wrinkly skin syndrome
Metageria
Hallermann-Streiff-François syndrome
Kindler syndrome
Bullous acrokeratotic poikiloderma of Kindler and Weary
Congenital poikiloderma with bullae and progressive cutaneous atrophy
Hereditary acrokeratotic poikiloderma
Weary–Kindler syndrome

后组配轴 Postcoordination

该条目未定义后组配轴，直接使用上面的编码即可。后组配是在主干编码之后追加侧别、具体解剖部位、严重程度、病因等细节的可选组合方式，不是必填项。