The Greig polysyndactyly-craniofacial dysmorphism syndrome.

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作者信息

Fryns J P, Coeck W, van den Berghe H

出版信息

Eur J Pediatr. 1977 Nov 4;126(4):283-7. doi: 10.1007/BF00477055.

DOI:10.1007/BF00477055

PMID:201464

Abstract

A 15-month-old male child with the Greig polysyndactyly-craniofacial dysmorphism syndrome is presented and the relevant literature is reviewed.

摘要

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The Greig polysyndactyly-craniofacial dysmorphism syndrome.

Eur J Pediatr. 1977 Nov 4;126(4):283-7. doi: 10.1007/BF00477055.

A newborn infant with craniofacial dysmorphism and polysyndactyly (Greig's syndrome).一名患有颅面畸形和多指（趾）畸形（Greig综合征）的新生儿。

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Eur J Pediatr. 1981 May;136(2):217-20. doi: 10.1007/BF00441928.

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[An unusual morbid association: oligophrenia with craniofacial dysmorphism (including hypertelorism), absence of the nails and terminal phalanges of the 4th and 5th fingers and other malformations in a 7-year-old girl].

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Unknown syndrome: abnormal facies, hypothyroidism, postaxial polydactyly, and severe retardation: a third patient.未知综合征：面容异常、甲状腺功能减退、轴后多指畸形及严重智力发育迟缓：第三例患者

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引用本文的文献

The spectrum of hand and foot malformations in patients with Greig cephalopolysyndactyly.Greig头多指（趾）畸形患者的手足畸形谱。

J Child Orthop. 2007 Jul;1(2):143-50. doi: 10.1007/s11832-007-0022-8. Epub 2007 May 10.

The Greig polysyndactyly craniofacial dysmorphism syndrome: variable expression in a family.格雷格多指（趾）并指（趾）颅面发育异常综合征：一个家族中的可变表现型

Eur J Pediatr. 1981 May;136(2):217-20. doi: 10.1007/BF00441928.

Greig syndrome associated with an interstitial deletion of 7p: confirmation of the localization of Greig syndrome to 7p13.与7号染色体短臂间质缺失相关的Greig综合征：Greig综合征定位于7p13的确认。

Hum Genet. 1991 Aug;87(4):452-6. doi: 10.1007/BF00197167.

本文引用的文献

Carpenter's syndrome: acrocephalopolysyndactyly. An autosomal recessive syndrome.

J Pediatr. 1966 Jul;69(1):111-20. doi: 10.1016/s0022-3476(66)80368-2.

Familial polysyndactyly and craniofacial anomalies.

Clin Genet. 1972;3(2):128-34. doi: 10.1111/j.1399-0004.1972.tb01734.x.

Frontodigital syndrome: a dominantly inherited disorder with normal intelligence.

J Pediatr. 1970 Jul;77(1):129-33. doi: 10.1016/s0022-3476(70)80058-0.

Acrocephalopolysyndactyly, type Noack, in a large kindred.

Birth Defects Orig Artic Ser. 1975;11(5):99-106.

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