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先天性手指屈曲综合征,瓜达拉哈拉2型

Camptodactyly syndrome, Guadalajara type 2

ORPHA:1326疾病

定义 英文原文(暂无中文)

Camptodactyly syndrome, Guadalajara type 2 is an extremely rare multiple congenital anomaly syndrome characterized by distinctive intrauterine growth retardation, skeletal dysplasia with multiple malformations including camptodactyly of all fingers, bilateral hallux valgus, short second, fourth and fifth toes, hypoplastic patella, microcephaly, low-set ears, short neck, cuboid-shaped vertebral bodies, pectus excavatum, hip dislocation, and hypoplastic pubic region and genitalia. Camptodactyly syndrome, Guadalajara type 2 has been described in two sisters and is most likely transmitted in an autosomal recessive manner. There have been no further descriptions in the literature since 1985.

基本事实

遗传方式
常染色体隐性
发病年龄
新生儿期
患病率
<1 / 1 000 000

临床表型 13

极常见 99–80%13

  • 手指弯曲 HP:0100490
  • 立方体形椎体 HP:0004634
  • 髋关节脱位 HP:0002827
  • 胎儿宫内发育迟缓 HP:0001511
  • 阴唇发育不良 HP:0000066
  • 小头畸形 HP:0000252
  • 髌骨发育不全 HP:0003065
  • 漏斗胸 HP:0000767
  • 第二趾短小 HP:0001885
  • 第三趾过短 HP:0005643
  • 第五趾短 HP:0011917
  • 身材矮小 HP:0004322
  • 马蹄内翻足 HP:0001762

外部标识与链接

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本页数据来源

  • 疾病定义、同义词、基因、表型、流行病学:Orphanet(CC BY 4.0)
  • 中文病名:Orphanet 中文包,冻结于 2020-06-01
  • 表型中文标签:HPO 简体中文翻译(CHPO 上游成果)