Literature DB >> 8500790

FFU complex: an analysis of 491 cases.

W Lenz1, M Zygulska, J Horst.   

Abstract

A study of 491 patients with femur-fibula-ulna (FFU) complex is presented. The term FFU complex has been proposed for cases in which the femur, fibula and/or ulna show defects, which tend to be associated. These cases are usually sporadic. Some rare anomalies of the arms which are present are particularly frequent in FFU complex. These are amelia, peromelia of humerus, humero-radial synostosis and defect of ulna. In our study, 491 patients were investigated for involvement of limb malformations. Our results, showing nearly equal proportions of the most common malformations in four analysed groups (with one, two, three and four limbs affected) supports the hypothesis that even if one arm or one leg only is affected, the cases may still be classifiable as FFU complex. There is a striking asymmetry in presence and in degree. All malformations are more often unilateral than bilateral. Upper limbs are affected more often than lower limbs. The right side and the male sex are preferentially affected. The limb malformations present in the FFU complex are different from those seen in most other types of limb defects, so there is virtually no overlap between FFU and other limb malformations. Some arguments in favour of early somatic mutation as a cause are discussed.

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Year:  1993        PMID: 8500790     DOI: 10.1007/BF00217355

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  13 in total

1.  Limb reduction defects and renal dysplasia: confirmation of a new, apparently lethal, autosomal recessive MCA syndrome.

Authors:  C Schrander-Stumpel; C de Die-Smulders; J P Fryns; J da Costa; P Bouckaert
Journal:  Am J Med Genet       Date:  1990-09

Review 2.  Fuhrmann syndrome of right-angle bowed femora, absence of fibulae and digital anomalies: two further cases.

Authors:  A H Lipson; K Kozlowski; A Barylak; W Marsden
Journal:  Am J Med Genet       Date:  1991-11-01

3.  Association of tetra-amelia, ectodermal dysplasia, hypoplastic lacrimal ducts and sacs opening towards the exterior, peculiar face, and developmental retardation.

Authors:  S Ohdo; H Madokoro; T Sonoda; M Takei; H Yasuda; N Mori
Journal:  J Med Genet       Date:  1987-10       Impact factor: 6.318

4.  Congenital absence of the fibula and craniosynostosis in sibs.

Authors:  R B Lowry
Journal:  J Med Genet       Date:  1972-06       Impact factor: 6.318

5.  Profound limb deficiency, thoracic dystrophy, unusual facies, and normal intelligence: a new syndrome.

Authors:  S A Al-Awadi; A S Teebi; T I Farag; K M Naguib; M Y el-Khalifa
Journal:  J Med Genet       Date:  1985-02       Impact factor: 6.318

6.  De novo 21q interstitial deletion in a retarded boy with ulno-fibular dysostosis.

Authors:  J F Reynolds; H E Wyandt; T E Kelly
Journal:  Am J Med Genet       Date:  1985-01

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

Authors:  D Kühne; W Lenz; D Petersen; H Schönenberg
Journal:  Humangenetik       Date:  1967

8.  Femoral hypoplasia-unusual facies syndrome in infants of diabetic mothers.

Authors:  J P Johnson; J C Carey; W M Gooch; J Petersen; J F Beattie
Journal:  J Pediatr       Date:  1983-06       Impact factor: 4.406

9.  Lethal form of fibuloulnar A/hypoplasia with renal abnormalities.

Authors:  N Saito; A Kuba; T Tsuruta
Journal:  Am J Med Genet       Date:  1989-04

10.  Tetra-amelia with multiple malformations in six male fetuses of one kindred.

Authors:  E Z Zimmer; E Taub; Y Sova; M Y Divon; M Pery; B A Peretz
Journal:  Eur J Pediatr       Date:  1985-11       Impact factor: 3.183

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  5 in total

1.  A rare association of congenital absence of femur and fibular hemimelia with maternal hyperpyrexia.

Authors:  Devendra Kumar; Sriram Krishnamurthy
Journal:  Indian J Pediatr       Date:  2009-11       Impact factor: 1.967

Review 2.  The two domain hypothesis of limb prepattern and its relevance to congenital limb anomalies.

Authors:  Hirotaka Tao; Yasuhiko Kawakami; Chi-Chung Hui; Sevan Hopyan
Journal:  Wiley Interdiscip Rev Dev Biol       Date:  2017-03-20       Impact factor: 5.814

3.  A case of severe proximal focal femoral deficiency with overlapping phenotypes of Al-Awadi-Raas-Rothschild syndrome and Fuhrmann syndrome.

Authors:  Masaki Matsushita; Hiroshi Kitoh; Kenichi Mishima; Yoshihiro Nishida; Naoki Ishiguro
Journal:  Pediatr Radiol       Date:  2014-05-18

4.  Asymmetrical tetraphocomelia with radiohumeral synostosis.

Authors:  Aderibigbe M Shonubi; Olutola Akiode; Babatunde A Salami; Adewale A Musa; Sikirat A Sotimehin; Ganiyu A Sule
Journal:  Ann Saudi Med       Date:  2006 Jul-Aug       Impact factor: 1.526

5.  Proximal femoral focal deficiency in a newborn.

Authors:  Zainab Babay
Journal:  Ann Saudi Med       Date:  2004 Nov-Dec       Impact factor: 1.526

  5 in total

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