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The Greig polysyndactyly-craniofacial dysmorphism syndrome.

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

相似文献

1
The Greig polysyndactyly-craniofacial dysmorphism syndrome.
Eur J Pediatr. 1977 Nov 4;126(4):283-7. doi: 10.1007/BF00477055.
2
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。
Acta Paediatr Scand. 1981 Mar;70(2):275-7. doi: 10.1111/j.1651-2227.1981.tb05557.x.
3
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.
4
Cranio-facial dysmorphism with digital abnormalities, oligophrenia and neurological disturbances--a variant of the Freeman-Sheldon syndrome?
Neurol Psychiatr (Bucur). 1975;13(2):127-32.
5
The occurrence of a fibro-osseous lesion and multiple dental anomalies in a patient with the Greig cephalopolysyndactyly syndrome.一名患有Greig头多指（趾）综合征的患者出现纤维性骨病变和多种牙齿异常。
Oral Surg Oral Med Oral Pathol. 1988 Oct;66(4):475-9. doi: 10.1016/0030-4220(88)90272-1.
6
[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].
Neurol Psihiatr Neurochir. 1973 May-Jun;18(3):255-62.
7
Schinzel acrocallosal syndrome: a variant example of the Greig syndrome?申泽尔综合征：格里格综合征的一种变异类型？
Ann Genet. 1985;28(4):239-40.
8
The Greig cephalopolysyndactyly syndrome: report of a family and review of the literature.格里格头多指（趾）综合征：一家系报告及文献复习
Am J Med Genet. 1985 Sep;22(1):59-68. doi: 10.1002/ajmg.1320220106.
9
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
J Med Genet. 1989 Dec;26(12):785-6. doi: 10.1136/jmg.26.12.785.
10
A new X linked syndrome with mental retardation and craniofacial dysmorphism?
J Med Genet. 1992 Oct;29(10):736-8. doi: 10.1136/jmg.29.10.736.

引用本文的文献

1
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.
2
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.
3
Greig syndrome associated with an interstitial deletion of 7p: confirmation of the localization of Greig syndrome to 7p13.

本文引用的文献

1
Carpenter's syndrome: acrocephalopolysyndactyly. An autosomal recessive syndrome.
J Pediatr. 1966 Jul;69(1):111-20. doi: 10.1016/s0022-3476(66)80368-2.
2
Familial polysyndactyly and craniofacial anomalies.
Clin Genet. 1972;3(2):128-34. doi: 10.1111/j.1399-0004.1972.tb01734.x.
3
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.
4
Acrocephalopolysyndactyly, type Noack, in a large kindred.
Birth Defects Orig Artic Ser. 1975;11(5):99-106.
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.