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Wallis–Zieff–Goldblatt syndrome is a rare condition characterized by inherited skeletal disorders manifested mainly as rhizomelic short stature and lateral clavicular defects. It is also known as Cleidorhizomelic syndrome.

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  • Wallis–Zieff–Goldblatt syndrome (en)
  • Wallis–Zieff–Goldblatt綜合症 (zh)
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  • Wallis–Zieff–Goldblatt syndrome is a rare condition characterized by inherited skeletal disorders manifested mainly as rhizomelic short stature and lateral clavicular defects. It is also known as Cleidorhizomelic syndrome. (en)
  • Wallis–Zieff–Goldblatt綜合症(Wallis–Zieff–Goldblatt syndrome),亦稱為Cleidorhizomelic綜合症(Cleidorhizomelic syndrome)是一種罕見的遺傳性骨骼疾病,由Wallis等在1988年12月首次報導,他們發現有一對母子患有這種遺傳性骨骼疾病,主要表現為肢根短小的身材(rhizomelic short stature)和側鎖骨的缺損。該綜合症的第一份臨床報告描述了一個6個月大的男孩,他的身材矮小且呈根狀,並且在鎖骨的側面有隆突。鎖骨外側的三分之一具有雙裂(bifid)的外觀,這是由異常過程或融合中心引起的隆凸(protuberance)所引致的結果。該男孩的母親時年22歲,身高142厘米,臂展136厘米,四肢短且呈根狀,出現異常。母子兩人雙手的手指都出現了一種稱為「」的彎曲情況,並且發現他們尾指的中節指骨發育不良。 (zh)
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  • Wallis–Zieff–Goldblatt syndrome (en)
name
  • Wallis–Zieff–Goldblatt syndrome (en)
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  • http://commons.wikimedia.org/wiki/Special:FilePath/Autosomal_dominant_-_en.svg
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ICD
  • Q77.8 (en)
OMIM
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  • Wallis–Zieff–Goldblatt syndrome has an autosomal dominant pattern of inheritance. (en)
synonyms
  • Cleidorhizomelic syndrome (en)
has abstract
  • Wallis–Zieff–Goldblatt syndrome is a rare condition characterized by inherited skeletal disorders manifested mainly as rhizomelic short stature and lateral clavicular defects. It is also known as Cleidorhizomelic syndrome. (en)
  • Wallis–Zieff–Goldblatt綜合症(Wallis–Zieff–Goldblatt syndrome),亦稱為Cleidorhizomelic綜合症(Cleidorhizomelic syndrome)是一種罕見的遺傳性骨骼疾病,由Wallis等在1988年12月首次報導,他們發現有一對母子患有這種遺傳性骨骼疾病,主要表現為肢根短小的身材(rhizomelic short stature)和側鎖骨的缺損。該綜合症的第一份臨床報告描述了一個6個月大的男孩,他的身材矮小且呈根狀,並且在鎖骨的側面有隆突。鎖骨外側的三分之一具有雙裂(bifid)的外觀,這是由異常過程或融合中心引起的隆凸(protuberance)所引致的結果。該男孩的母親時年22歲,身高142厘米,臂展136厘米,四肢短且呈根狀,出現異常。母子兩人雙手的手指都出現了一種稱為「」的彎曲情況,並且發現他們尾指的中節指骨發育不良。 (zh)
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ICD10
  • Q77.8
OMIM id
ORPHA
  • 1453
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