Literature DB >> 6288948

Familial Poland anomaly.

T J David.   

Abstract

The Poland anomaly is usually a non-genetic malformation syndrome. This paper reports two second cousins who both had a typical left sided Poland anomaly, and this constitutes the first recorded case of this condition affecting more than one member of a family. Despite this, for the purposes of genetic counselling, the Poland anomaly can be regarded as a sporadic condition with an extremely low recurrence risk.

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Year:  1982        PMID: 6288948      PMCID: PMC1048897          DOI: 10.1136/jmg.19.4.293

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  11 in total

1.  The familial occurrence of Poland syndrome.

Authors:  E Sujansky; V M Riccardi; A L Matthew
Journal:  Birth Defects Orig Artic Ser       Date:  1977

2.  Risk of recurrence in usually nongenetic malformation syndromes.

Authors:  R J Gorlin
Journal:  Birth Defects Orig Artic Ser       Date:  1979

3.  Poland syndrome in British Columbia: incidence and reproductive experience of affected persons.

Authors:  B C McGillivray; R B Lowry
Journal:  Am J Med Genet       Date:  1977

4.  Nature and etiology of the Poland anomaly.

Authors:  T J David
Journal:  N Engl J Med       Date:  1972-09-07       Impact factor: 91.245

5.  [Clinical and genetic aspects of Poland's syndrome].

Authors:  W Fuhrmann; U Mösseler; H Neuss
Journal:  Dtsch Med Wochenschr       Date:  1971-06-18       Impact factor: 0.628

6.  Vascular origin of Poland syndrome? by J.-P. Bouvet et al.

Authors:  T J David
Journal:  Eur J Pediatr       Date:  1979-04-03       Impact factor: 3.183

7.  Letter: Absence of pectoralis major muscle in two sisters associated with leukemia in one of them.

Authors:  S Armendares
Journal:  J Pediatr       Date:  1974-09       Impact factor: 4.406

8.  The IVIC syndrome: a new autosomal dominant complex pleiotropic syndrome with radial ray hypoplasia, hearing impairment, external ophthalmoplegia, and thrombocytopenia.

Authors:  S Arias; V B Penchaszadeh; J Pinto-Cisternas; S Larrauri
Journal:  Am J Med Genet       Date:  1980

9.  Poland's syndrome.

Authors:  D C Ireland; N Takayama; A E Flatt
Journal:  J Bone Joint Surg Am       Date:  1976-01       Impact factor: 5.284

10.  [Congenital dysplasia of the musculi pectorales associated with congenital hand and finger malformations of the ipsilateral upper limb].

Authors:  K Trosev; J Cervenka; E Gerberová
Journal:  Acta Chir Orthop Traumatol Cech       Date:  1966-08       Impact factor: 0.531

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  7 in total

Review 1.  Presentation and Treatment of Poland Anomaly.

Authors:  Joseph A Buckwalter V; Apurva S Shah
Journal:  Hand (N Y)       Date:  2016-10-10

2.  Muscle abnormalities of the chest in Poland's syndrome: variations and proposal for a classification.

Authors:  Kapetanakis Stylianos; Papadopoulos Constantinos; Triantafilidis Alexandros; Fiska Aliki; Agrogiannis Nikolaos; Maria Demetriou; Panagiotou Petros
Journal:  Surg Radiol Anat       Date:  2011-07-29       Impact factor: 1.246

3.  Familial Poland anomaly.

Authors:  R B Lowry; J P Bouvet
Journal:  J Med Genet       Date:  1983-04       Impact factor: 6.318

4.  Neurofibroma and Pectoralis Muscle Hypoplasia: A Mild Degree of Poland's Syndrome.

Authors:  Caiping Chen; Jianju Lu; Xiang Lu; Wanxin Wu; Wenlan Han
Journal:  Breast Care (Basel)       Date:  2012-12       Impact factor: 2.860

5.  Familial absence of the pectoralis major, serratus anterior, and latissimus dorsi muscles.

Authors:  T J David; R M Winter
Journal:  J Med Genet       Date:  1985-10       Impact factor: 6.318

6.  A case report of Poland Syndrome with Absent Limb Anomalies.

Authors:  Abhinav D Jogani; Prakash K George; Nandan A Marathe; Swapneel S Shah; Jigar R Desai
Journal:  J Orthop Case Rep       Date:  2019

7.  Poland syndrome accompanied by internal iliac artery supply disruption sequence: a case report.

Authors:  Kenji Gonda; Yosuke Tachiya; Yuichi Hatakeyama; Tomoyuki Momma; Tomoko Tamaoki; Yuko Maejima; Yuichi Rokkaku; Shigehira Saji; Kenju Shimomura; Koji Kono
Journal:  J Med Case Rep       Date:  2018-10-26
  7 in total

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