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Year : 2015  |  Volume : 4  |  Issue : 4  |  Page : 285-287

Larsen syndrome: Image in clinical neonatology

1 Neonatologist, ian Royal Medical Services, Amman, Jordan
2 Department of Paediatric, G.P., Jordanian Royal Medical Services, Amman, Jordan
3 Department of Pediatrician, Jordanian Royal Medical Services, Amman, Jordan

Correspondence Address:
Ghassan S. A. Salama
Senior Specialist of Neonatology, Pediatric Department, Division of Neonatology, Jordanian Royal Medical Services, Amman
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Source of Support: None, Conflict of Interest: None

DOI: 10.4103/2249-4847.161716

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Larsen syndrome (LS) is a rare osteochondrodysplastic genetic disorder. The cardinal features of this condition are dislocations of the large joints, skeletal malformations, and the distinctive facial features. Here, we are presenting the features of LS in a full term female newborn.

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