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Asymmetrical tetraphocomelia with radiohumeral synostosis.

作者信息

Shonubi Aderibigbe M, Akiode Olutola, Salami Babatunde A, Musa Adewale A, Sotimehin Sikirat A, Sule Ganiyu A

机构信息

Queen Elizabeth II Hospital, Maseru, Lesotho.

出版信息

Ann Saudi Med. 2006 Jul-Aug;26(4):318-20. doi: 10.5144/0256-4947.2006.318.

DOI:10.5144/0256-4947.2006.318

PMID:16885632

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6074508/

Abstract

摘要

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a52/6074508/156d44c34653/asm-4-318f1.jpg

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Asymmetrical tetraphocomelia with radiohumeral synostosis.

Ann Saudi Med. 2006 Jul-Aug;26(4):318-20. doi: 10.5144/0256-4947.2006.318.

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[Defects of the femur and fibula with amelia, peromelia or ulnar defects of the arm. A syndrome].

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[Characteristics of certain types of limb reduction abnormalities].

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[Congenital radioulnar synostosis].

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[A case of congenital bilateral radio-ulnar synostosis].

Rev Cubana Pediatr. 1953 Mar;25(3):171-3.

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Arch Ortop. 1959;72:1246-53.

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本文引用的文献

Sirenomelia in one of Nigerian monochorionic twins.

Afr J Med Med Sci. 2002 Dec;31(4):377-9.

Upper-extremity congenital anomalies.

J Bone Joint Surg Am. 2003 Aug;85(8):1564-76. doi: 10.2106/00004623-200308000-00021.

Humeroradial synostosis, ulnar aplasia and oligodactyly, with contralateral amelia, in a child with prenatal cocaine exposure.

Am J Med Genet A. 2003 Jan 1;116A(1):85-9. doi: 10.1002/ajmg.a.10731.

Symmetrical tetraphocomelia without associated congenital malformations: a nosological dilemma.

Am J Med Genet. 2002 Nov 22;113(2):227-8. doi: 10.1002/ajmg.10678.

New case of bilateral upper limb amelia, facial clefts, and renal hypoplasia.

Am J Med Genet. 2000 Mar 13;91(2):123-5. doi: 10.1002/(sici)1096-8628(20000313)91:2<123::aid-ajmg8>3.0.co;2-n.

FFU complex: an analysis of 491 cases.

Hum Genet. 1993 May;91(4):347-56. doi: 10.1007/BF00217355.

Roberts syndrome: a review of 100 cases and a new rating system for severity.

Am J Med Genet. 1993 Nov 15;47(7):1104-23. doi: 10.1002/ajmg.1320470735.

Tetra-amelia, lung hypo-/aplasia, cleft lip-palate, and heart defect: a new syndrome?

Am J Med Genet. 1994 May 15;51(1):77-80. doi: 10.1002/ajmg.1320510116.

New autosomal recessive form of amelia.

Am J Med Genet. 1995 Mar 27;56(2):164-7. doi: 10.1002/ajmg.1320560210.

Prenatal diagnosis of Roberts syndrome.

Prenat Diagn. 1994 Jun;14(6):511-2. doi: 10.1002/pd.1970140618.

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相似文献

Asymmetrical tetraphocomelia with radiohumeral synostosis.

Ann Saudi Med. 2006 Jul-Aug;26(4):318-20. doi: 10.5144/0256-4947.2006.318.

Humeroradioulnar synostosis in a patient with lambdoid synostosis.

J Med Genet. 1993 Jan;30(1):81-2. doi: 10.1136/jmg.30.1.81.

Further report of a patient with humeroradioulnar synostosis and hydronephrosis.

J Med Genet. 1995 Jan;32(1):78-9. doi: 10.1136/jmg.32.1.78-a.

[Defects of the femur and fibula with amelia, peromelia or ulnar defects of the arm. A syndrome].

Humangenetik. 1967;3(3):244-63. doi: 10.1007/BF00273126.

[Characteristics of certain types of limb reduction abnormalities].

Orv Hetil. 1985 Aug 4;126(31):1917-20.

Antley-Bixler syndrome with radioulnar synostosis.

Pediatr Radiol. 2004 Feb;34(2):148-51. doi: 10.1007/s00247-003-1066-7. Epub 2003 Sep 26.

[Congenital radioulnar synostosis].

Rev Clin Esp. 1956 Apr 15;61(1):44-6.

[A case of congenital bilateral radio-ulnar synostosis].

Rev Cubana Pediatr. 1953 Mar;25(3):171-3.

[On a case of congenital radio-ulnar synostosis treated surgically].

Arch Ortop. 1959;72:1246-53.

Radioulnar synostosis in Williams syndrome: a historical overview.

Am J Med Genet. 1994 May 1;50(4):386. doi: 10.1002/ajmg.1320500421.

本文引用的文献

Sirenomelia in one of Nigerian monochorionic twins.

Afr J Med Med Sci. 2002 Dec;31(4):377-9.

Upper-extremity congenital anomalies.

J Bone Joint Surg Am. 2003 Aug;85(8):1564-76. doi: 10.2106/00004623-200308000-00021.

Humeroradial synostosis, ulnar aplasia and oligodactyly, with contralateral amelia, in a child with prenatal cocaine exposure.

Am J Med Genet A. 2003 Jan 1;116A(1):85-9. doi: 10.1002/ajmg.a.10731.

Symmetrical tetraphocomelia without associated congenital malformations: a nosological dilemma.

Am J Med Genet. 2002 Nov 22;113(2):227-8. doi: 10.1002/ajmg.10678.

New case of bilateral upper limb amelia, facial clefts, and renal hypoplasia.

Am J Med Genet. 2000 Mar 13;91(2):123-5. doi: 10.1002/(sici)1096-8628(20000313)91:2<123::aid-ajmg8>3.0.co;2-n.

FFU complex: an analysis of 491 cases.

Hum Genet. 1993 May;91(4):347-56. doi: 10.1007/BF00217355.

Roberts syndrome: a review of 100 cases and a new rating system for severity.

Am J Med Genet. 1993 Nov 15;47(7):1104-23. doi: 10.1002/ajmg.1320470735.

Tetra-amelia, lung hypo-/aplasia, cleft lip-palate, and heart defect: a new syndrome?

Am J Med Genet. 1994 May 15;51(1):77-80. doi: 10.1002/ajmg.1320510116.

New autosomal recessive form of amelia.

Am J Med Genet. 1995 Mar 27;56(2):164-7. doi: 10.1002/ajmg.1320560210.

Prenatal diagnosis of Roberts syndrome.

Prenat Diagn. 1994 Jun;14(6):511-2. doi: 10.1002/pd.1970140618.