Femoral‐facial syndrome: A review of the literature and 14 additional patients including a monozygotic discordant twin pair

Author:

Lacarrubba‐Flores Maria Dora Jazmin12ORCID,Carvalho Daniel Rocha3,Ribeiro Erlane Marques4,Moreno Carolina Araujo12,Esposito Ana Carolina5,Marson Fernando Augusto Lima6ORCID,Loureiro Thereza7,Cavalcanti Denise Pontes12ORCID

Affiliation:

1. Skeletal Dysplasia Group, Department of Medical Genetics, Faculty of Medical SciencesUniversity of Campinas [Unicamp] Campinas, São Paulo Brazil

2. Perinatal Genetic Program, Department of Medical Genetics, Faculty of Medical SciencesUniversity of Campinas [Unicamp] Campinas, São Paulo Brazil

3. Genetic Unit, SARAH Network of Rehabilitation HospitalFederal District Brasilia Brazil

4. Department of PediatricsChildren's Hospital Albert Sabin Fortaleza Ceará Brazil

5. Pediatric DivisionHospital Municipal Nossa Senhora do Loreto Rio de Janeiro Brazil

6. Department of Pediatrics, Faculty of Medical Sciences, University of Campinas [Unicamp] Campinas, São Paulo Brazil

7. Unit of Medical Genetics, Department of Genetics, Faculty of Medicine, University of São Paulo Riberão Preto, São Paulo Brazil

Funder

Conselho Nacional de Desenvolvimento Científico e Tecnológico

Fundação de Amparo à Pesquisa do Estado de São Paulo

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference109 articles.

1. Congenital malformations among infants whose mothers had gestational diabetes or preexisting diabetes

2. Congenital absence of femur and fibula;Acker R. B.;Report of two cases. Clinical Orthopaedics,1959

3. Preaxial hallucal polydactyly as a marker for diabetic embryopathy

4. Femoral–facial syndrome in an infant of a diabetic mother

5. Femoral hypoplasia‐unusual facies syndrome with renal agenesis and patent ductus arteriosus;Aksoy H. T.;Genetic Counseling,2013

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