Literature DB >> 22068244

A review of supernumerary and absent limbs and digits of the upper limb.

Zachary Klaassen1, Monica Choi, Ruth Musselman, Deborah Eapen, R Shane Tubbs, Marios Loukas.   

Abstract

For years people have been enamored by anomalies of the human limbs, particularly supernumerary and absent limbs and digits. Historically, there are a number of examples of such anomalies, including royal families of ancient Chaldea, tribes from Arabia, and examples from across nineteenth century Europe. The development of the upper limbs in a growing embryo is still being elucidated with the recent advent of homeobox genes, but researchers agree that upper limbs develop between stages 12-23 through a complex embryological process. Maternal thalidomide intake during limb development is known to cause limb reduction and subsequent amelia or phocomelia. Additionally, a number of clinical reports have illustrated different limb anomaly cases, with each situation unique in phenotype and developmental abnormality. Supernumerary and absent limbs and digits are not unique to humans, and a number of animal cases have also been reported. This review of the literature illustrates the historical, anatomical, and clinical aspects of supernumerary and absent limbs and digits for the upper limb.

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Year:  2011        PMID: 22068244     DOI: 10.1007/s00276-011-0871-1

Source DB:  PubMed          Journal:  Surg Radiol Anat        ISSN: 0930-1038            Impact factor:   1.246


  33 in total

Review 1.  Surgical excision of pedunculated supernumerary digits prevents traumatic amputation neuromas.

Authors:  Geoffrey E Leber; Arun K Gosain
Journal:  Pediatr Dermatol       Date:  2003 Mar-Apr       Impact factor: 1.588

2.  Roberts syndrome or "X-linked amelia"?

Authors:  R Gershoni-Baruch; A Drugan; M Bronshtein; E Z Zimmer
Journal:  Am J Med Genet       Date:  1990-12

3.  Bilateral hands and feet postaxial polydactyly presenting with renal vascular anomalies.

Authors:  Ainory Peter Gesase
Journal:  Ital J Anat Embryol       Date:  2006 Oct-Dec

4.  Accessory arm--dysraphism or disparity? Case report.

Authors:  R P Humphreys; K H Manwaring; N C Carroll
Journal:  J Neurosurg       Date:  1991-02       Impact factor: 5.115

5.  Syndrome of tetraamelia with pulmonary hypoplasia.

Authors:  J Zlotogora; M Sagi; Y O Shabany; R Y Jarallah
Journal:  Am J Med Genet       Date:  1993-09-15

6.  Four siblings with Robert's syndrome.

Authors:  L Zergollern; V Hitrec
Journal:  Clin Genet       Date:  1982-01       Impact factor: 4.438

7.  Subtotal amelia in a child with autosomal recessive hypohidrotic ectodermal dysplasia.

Authors:  Ali Al Kaissi; Farid Ben Chehida; Nabil Nassib; Hatem Safi; Mrad Djnziri; Maher Ben Ghachem; Hassan Gharbi
Journal:  Afr Health Sci       Date:  2005-09       Impact factor: 0.927

8.  Skeletal anomalies and deformities in patients with deletions of 22q11.

Authors:  J E Ming; D M McDonald-McGinn; T E Megerian; D A Driscoll; E R Elias; B M Russell; M Irons; B S Emanuel; R I Markowitz; E H Zackai
Journal:  Am J Med Genet       Date:  1997-10-17

Review 9.  Midline dorsal appendages.

Authors:  B B Fulmer; R H Wilkins; W J Oakes; H C Filston
Journal:  Pediatr Neurosurg       Date:  1997-11       Impact factor: 1.162

10.  Homozygous WNT3 mutation causes tetra-amelia in a large consanguineous family.

Authors:  Stephan Niemann; Chengfeng Zhao; Filon Pascu; Ulrich Stahl; Ute Aulepp; Lee Niswander; James L Weber; Ulrich Müller
Journal:  Am J Hum Genet       Date:  2004-02-05       Impact factor: 11.025

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  1 in total

1.  Amelia: A Case Report and Literature Review.

Authors:  Fatemeh Eghbalian; Amine Sharif; Amir Reza Monsef
Journal:  Iran J Pediatr       Date:  2015-12-23       Impact factor: 0.364

  1 in total

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