Literature DB >> 21886738

Sporadic familial ulnar hexadactyly of all four limbs.

Uwe Wollina1, Shyam B Verma.   

Abstract

BACKGROUND: Polydactyly belongs to skeletal anomalies and may be a symptom of more complex genetic syndromes. MAIN OBSERVATION: We observed an index case of ulnar hexadactyly of all four limbs in a 20-year-old man from India with three more brothers affected in his family. No additional anomalies were observed. The diagnosis of a sporadic (ulnar) postaxial hexadactyly was made.
CONCLUSION: Sporadic postaxial hexadactyly is one of the most common polydactylies in humans. In contrast, in the dermatologic literature the condition has only rarely been described.
CONCLUSION: Presence of supernummary digits or toes, i.e. polydactyly, is seen occasionally in the dermatologic practise. The present case is extraordinary since all limbs were involved and the same was true for three of his brothers. If treatment is asked, hand surgery would be necessary.

Entities:  

Keywords:  hexadactyly; polydactyly

Year:  2010        PMID: 21886738      PMCID: PMC3157808          DOI: 10.3315/jdcr.2010.1042

Source DB:  PubMed          Journal:  J Dermatol Case Rep        ISSN: 1898-7249


  27 in total

1.  [Hexadactylism of the four limbs: a case report].

Authors:  M C Villa; A Rocca; A Kantar; C Lovati; F Porcelli
Journal:  Pediatr Med Chir       Date:  2006

2.  [Polydactyly: a genetic epidemiological study in Santiago, Chile].

Authors:  L Cifuentes; J Nazer; M E Hüber; R Ramírez; C Nazer; I Morales
Journal:  Rev Med Chil       Date:  1996-03       Impact factor: 0.553

3.  Polydactyly: a study of four generations of a Turkish family including an affected member with bilateral cleft lip and palate.

Authors:  Uğur Koçer; Hasan M Aksoy; Yiğit O Tiftikcioğlu; Onder Karaaslan
Journal:  Scand J Plast Reconstr Surg Hand Surg       Date:  2002

4.  [Polydactyly in 26,670 consecutive births. The clinical characteristics, prevalence and risk factors].

Authors:  J J Pérez-Molina; N Alfaro-Alfaro; M C López-Zermeño; M A García-Calderón
Journal:  Bol Med Hosp Infant Mex       Date:  1993-11

5.  [Hexadactyly of hand and feet in a patient with basal cell nevus syndrome].

Authors:  E Hermes; T Liekenbröcker; M Körner; A Kapp; B Wedi
Journal:  Hautarzt       Date:  2002-10       Impact factor: 0.751

6.  McKusik-Kaufman syndrome: prenatal diagnosis, genetics and follow up.

Authors:  Pascal Gaucherand; Chantal Vavasseur-Monot; Elizabeth Ollagnon; Catherine Boisson; Jean-Marc Labaune; Thierry Basset; George Yared
Journal:  Prenat Diagn       Date:  2002-11       Impact factor: 3.050

7.  De novo t(12;17)(p13.3;q21.3) translocation with a breakpoint near the 5' end of the HOXB gene cluster in a patient with developmental delay and skeletal malformations.

Authors:  Ying Yue; Ruxandra Farcas; Gundula Thiel; Christiane Bommer; Bärbel Grossmann; Danuta Galetzka; Christina Kelbova; Peter Küpferling; Angelika Daser; Ulrich Zechner; Thomas Haaf
Journal:  Eur J Hum Genet       Date:  2007-02-28       Impact factor: 4.246

8.  Polysyndactyly, complex heart malformations cardiopathy, and hepatic ductal plate anomalies: an autosomal recessive syndrome diagnosed antenatally.

Authors:  Claude Stoll; B Gasser
Journal:  Am J Med Genet A       Date:  2003-06-01       Impact factor: 2.802

Review 9.  A multiple translocation event in a patient with hexadactyly, facial dysmorphism, mental retardation and behaviour disorder characterised comprehensively by molecular cytogenetics. Case report and review of the literature.

Authors:  Jörg Seidel; Anita Heller; Gabriele Senger; Heike Starke; Ilse Chudoba; Christina Kelbova; Holger Tönnies; Heidemarie Neitzel; Claudia Haase; Volkmar Beensen; Felix Zintl; Uwe Claussen; Thomas Liehr
Journal:  Eur J Pediatr       Date:  2003-06-19       Impact factor: 3.183

Review 10.  Ellis-van Creveld syndrome.

Authors:  Geneviève Baujat; Martine Le Merrer
Journal:  Orphanet J Rare Dis       Date:  2007-06-04       Impact factor: 4.123

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