Literature DB >> 19308564

Epidemiology, etiology, and genetic aspects of reduction deficiencies of the lower limb.

Ismat Ghanem1.   

Abstract

Although the majority of lower limb deficiencies are of sporadic occurrence and of unknown etiology, genetic factors are involved in a significant number, with variable modes of inheritance. A better-informed public is demanding advice concerning cause and recurrence. Careful scrutiny of the medical history and family tree and attention to phenotypic details may help to delineate entities. At times, specific chromosomal tests are important, mainly when there is bilateral or multiorgan involvement or when limb deficiency is associated with developmental delay and/or mental retardation. This paper is intended to refamiliarize the orthopaedic community with basic genetic aspects regulating reduction deficiencies of the lower limbs, and to emphasize on the importance and indications of genetic counseling.

Entities:  

Year:  2008        PMID: 19308564      PMCID: PMC2656849          DOI: 10.1007/s11832-008-0098-9

Source DB:  PubMed          Journal:  J Child Orthop        ISSN: 1863-2521            Impact factor:   1.548


  20 in total

1.  Tibial/femoral hypoplasia with "hook" pelvis: a potentially unique dysostosis.

Authors:  André Mégarbané; Ismat Ghanem
Journal:  Am J Med Genet       Date:  2002-11-01

2.  Prenatal growth deficiency with narrowness of the cervical spine, subglottic stenosis, hip dislocation, and severe delayed bone ossification: a new skeletal dysplasia.

Authors:  André Mégarbané; Ismat Ghanem; Tony Rizk; Pascal Jabbour
Journal:  Am J Med Genet       Date:  2002-09-15

3.  A newly recognized chondrodysplasia with multiple dislocations.

Authors:  André Mégarbané; Ismat Ghanem
Journal:  Am J Med Genet A       Date:  2004-09-15       Impact factor: 2.802

4.  Genomewide linkage scan for split-hand/foot malformation with long-bone deficiency in a large Arab family identifies two novel susceptibility loci on chromosomes 1q42.2-q43 and 6q14.1.

Authors:  Mohammed Naveed; Swapan K Nath; Mathew Gaines; Mahmoud T Al-Ali; Najib Al-Khaja; David Hutchings; Jeffrey Golla; Samuel Deutsch; Armand Bottani; Stylianos E Antonarakis; Uppala Ratnamala; Uppala Radhakrishna
Journal:  Am J Hum Genet       Date:  2006-11-29       Impact factor: 11.025

5.  Ectrodactyly with aplasia of long bones (OMIM; 119100) in a large inbred Arab family with an apparent autosomal dominant inheritance and reduced penetrance: clinical and genetic analysis.

Authors:  Mohammed Naveed; Mahmoud T Al-Ali; Sabita K Murthy; Sarah Al-Hajali; Najib Al-Khaja; Samuel Deutsch; Armand Bottani; Stylianos E Antonarakis; Swapan K Nath; Uppala Radhakrishna
Journal:  Am J Med Genet A       Date:  2006-07-01       Impact factor: 2.802

6.  Congenital limb anomalies:frequency and aetiological factors. Data from the Edinburgh Register of the Newborn (1964-68).

Authors:  E J Rogala; R Wynne-Davies; A Littlejohn; J Gormley
Journal:  J Med Genet       Date:  1974-09       Impact factor: 6.318

7.  Hereditary congenital coxa vara with dominant inheritance?

Authors:  B Say; E Tunçbilek; T Pirnar; N Tokgözoglu
Journal:  Humangenetik       Date:  1971

8.  Familial limb deficiency.

Authors:  A Hoon; J G Hall
Journal:  Clin Genet       Date:  1988-08       Impact factor: 4.438

9.  A pair of sibs with tibial hemimelia born to phenotypically normal parents.

Authors:  Juntaro Matsuyama; Akihiko Mabuchi; Junwei Zhang; Aritoshi Iida; Toshiyuki Ikeda; Mamori Kimizuka; Shiro Ikegawa
Journal:  J Hum Genet       Date:  2003-03-11       Impact factor: 3.172

10.  Tibial hemimelia-cleft lip/palate in a Brazilian child born to consanguineous parents.

Authors:  A Richieri-Costa
Journal:  Am J Med Genet       Date:  1987-10
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  1 in total

1.  Upper limb hemimelia in a twin pregnancy which was obtained by an ICSI and PGD in a woman with mosaic Turner's syndrome and the prognosis.

Authors:  Ahter Tanay Tayyar; Ahmet Tayyar; Ahmet Eser; Çetin Kılıçcı; İlter Yenidede; Selçuk Selçuk
Journal:  Organogenesis       Date:  2017-09-21       Impact factor: 2.500

  1 in total

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