Management of Patella Dislocation in Say-Barber-Biesecker-Young-Simpson’s Syndrome: A Report of Two Cases

Say-Barber-Biesecker-Young-Simpson’s syndrome is one of the Ohdo-like syndromes. It is a very rare congenital condition that is commonly defined by its main clinical features that are blepharophimosis, ptosis, mental retardation, and delayed motor development. They are often associated with skeletal...

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Main Authors: Meni Mundama, Serge Ayong, Renaud Rossillon
Format: Article
Language:English
Published: Hindawi Limited 2018-01-01
Series:Case Reports in Orthopedics
Online Access:http://dx.doi.org/10.1155/2018/6415713
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spelling doaj-ef59720267bd4041aa3175ba1f90a24b2020-11-24T21:28:59ZengHindawi LimitedCase Reports in Orthopedics2090-67492090-67572018-01-01201810.1155/2018/64157136415713Management of Patella Dislocation in Say-Barber-Biesecker-Young-Simpson’s Syndrome: A Report of Two CasesMeni Mundama0Serge Ayong1Renaud Rossillon2Department of Orthopaedic Surgery, Clinique Saint-Pierre Ottignies, Avenue Reine Fabiola 9, 1340 Ottignies, BelgiumDepartment of Orthopaedic Surgery, Clinique Saint-Pierre Ottignies, Avenue Reine Fabiola 9, 1340 Ottignies, BelgiumDepartment of Orthopaedic Surgery, Clinique Saint-Pierre Ottignies, Avenue Reine Fabiola 9, 1340 Ottignies, BelgiumSay-Barber-Biesecker-Young-Simpson’s syndrome is one of the Ohdo-like syndromes. It is a very rare congenital condition that is commonly defined by its main clinical features that are blepharophimosis, ptosis, mental retardation, and delayed motor development. They are often associated with skeletal manifestations that are joint laxity, long thumbs and toes, and hypoplastic and/or dislocated patellae. To our knowledge, the available literature does not report any case where attention is drawn to management of skeletal aspect of this specific syndrome, especially surgically. We report 2 cases of SBBYS syndrome with patellar dislocation that we followed for 11 years. One case (with bilateral dislocation) was managed conservatively, and the other (with unilateral dislocation) underwent conservative and surgical treatment. Both had good functional outcome at follow-up. This experience shows that patellar abnormality in this condition can be efficiently addressed conservatively and/or surgically with satisfying results.http://dx.doi.org/10.1155/2018/6415713
collection DOAJ
language English
format Article
sources DOAJ
author Meni Mundama
Serge Ayong
Renaud Rossillon
spellingShingle Meni Mundama
Serge Ayong
Renaud Rossillon
Management of Patella Dislocation in Say-Barber-Biesecker-Young-Simpson’s Syndrome: A Report of Two Cases
Case Reports in Orthopedics
author_facet Meni Mundama
Serge Ayong
Renaud Rossillon
author_sort Meni Mundama
title Management of Patella Dislocation in Say-Barber-Biesecker-Young-Simpson’s Syndrome: A Report of Two Cases
title_short Management of Patella Dislocation in Say-Barber-Biesecker-Young-Simpson’s Syndrome: A Report of Two Cases
title_full Management of Patella Dislocation in Say-Barber-Biesecker-Young-Simpson’s Syndrome: A Report of Two Cases
title_fullStr Management of Patella Dislocation in Say-Barber-Biesecker-Young-Simpson’s Syndrome: A Report of Two Cases
title_full_unstemmed Management of Patella Dislocation in Say-Barber-Biesecker-Young-Simpson’s Syndrome: A Report of Two Cases
title_sort management of patella dislocation in say-barber-biesecker-young-simpson’s syndrome: a report of two cases
publisher Hindawi Limited
series Case Reports in Orthopedics
issn 2090-6749
2090-6757
publishDate 2018-01-01
description Say-Barber-Biesecker-Young-Simpson’s syndrome is one of the Ohdo-like syndromes. It is a very rare congenital condition that is commonly defined by its main clinical features that are blepharophimosis, ptosis, mental retardation, and delayed motor development. They are often associated with skeletal manifestations that are joint laxity, long thumbs and toes, and hypoplastic and/or dislocated patellae. To our knowledge, the available literature does not report any case where attention is drawn to management of skeletal aspect of this specific syndrome, especially surgically. We report 2 cases of SBBYS syndrome with patellar dislocation that we followed for 11 years. One case (with bilateral dislocation) was managed conservatively, and the other (with unilateral dislocation) underwent conservative and surgical treatment. Both had good functional outcome at follow-up. This experience shows that patellar abnormality in this condition can be efficiently addressed conservatively and/or surgically with satisfying results.
url http://dx.doi.org/10.1155/2018/6415713
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