Literature DB >> 12868468

Fuhrmann syndrome: two Brazilian cases.

J Huber1, J B Volpon, E S Ramos.   

Abstract

We describe two unrelated boys with bilateral fibula aplasia, poly- and oligodactyly, and bowed tibiae in two non-consanguineous Brazilian families. These cases are similar to those reported by Fuhrman et al. [(1980). Skeletal Dysplasias. New York: Alan R. Liss Inc. pp. 519-524].

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Year:  2003        PMID： 12868468     DOI： 10.1097/00019605-200304000-00002

Source DB:  PubMed          Journal:  Clin Dysmorphol        ISSN： 0962-8827            Impact factor:   0.816


  3 in total

1.  A Turkish Female Twin Sister Patient with Fibular Aplasia, Congenital Tibia Pseudoarthrosis, Oligosyndactyly, and Negative WNT7A Gene Mutation.

Authors:  Hale Önder Yılmaz; Duran Topak; Orkun Yılmaz; Seda Çakmaklı
Journal:  J Pediatr Genet       Date:  2018-11-18

2.  A Female Newborn Infant with FATCO Syndrome Variant (Fibular Hypoplasia, Tibial Campomelia, Oligosyndactyly) - A Case Report.

Authors:  Gitte Smets; Yoeri Vankan; Annick Demeyere
Journal:  J Belg Soc Radiol       Date:  2016-02-26       Impact factor: 1.894

3.  Newborn Male With Fibular Aplasia, Tibial Campomelia, and Oligosyndactyly Syndrome: A New Case Report Putting the Condition Under Spotlight.

Authors:  Marian K Georgeos; Dina R Elgzzar
Journal:  Cureus       Date:  2022-01-28
  3 in total

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