A Case Report of Jarcho–Levin Syndrome and Caudal Regression Syndrome in A Five Year Old Girl

Introduction: Jarcho- Levin syndrome and caudal regression syndrome are rare syndromes with clinical and radiologic findings of cervical and thoracic vertebral anomalies with rib deformities (jarcho-levin syndrome) and sacrococcygeal agenesis, lower extremity anomalies, truncated spinal cord and neu...

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Main Authors: Hosein Emad Momtaz, Mahmood Jabbari
Format: Article
Language:fas
Published: Hamadan University of Medical Sciences 2008-09-01
Series:پزشکی بالینی ابن سینا
Subjects:
Online Access:http://sjh.umsha.ac.ir/article-1-375-en.html
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spelling doaj-90cf9799ab254053a8319ae7a2a8151d2020-11-25T04:11:23ZfasHamadan University of Medical Sciencesپزشکی بالینی ابن سینا2588-722X2588-72382008-09-011527073A Case Report of Jarcho–Levin Syndrome and Caudal Regression Syndrome in A Five Year Old GirlHosein Emad Momtaz0Mahmood Jabbari1 Introduction: Jarcho- Levin syndrome and caudal regression syndrome are rare syndromes with clinical and radiologic findings of cervical and thoracic vertebral anomalies with rib deformities (jarcho-levin syndrome) and sacrococcygeal agenesis, lower extremity anomalies, truncated spinal cord and neurogenic bladder (caudal regression syndrome). There are only one report of simultaneous existence of these two syndromes in a dead fetus in literature. Case Report: The case was a 5 year old girl who had history of bilateral hip dysplasia and spastic dipleigia of lower limbs who presented with recurrent urinary tract infections. X - Ray findings was extensive vertebral anomalies such as hemivertebrae, butterfly vertebrae, coccygeal agenesis and rib deformities. MRI findings was termination of spinal cord at low thoracic level, cystic mass of sacral area. Conclusion: This case is a rare simultaneous occurrence of Jarcho-levin and Cauda regression syndrome in a patient and to our best knowledge is reported for the first time in Iran.http://sjh.umsha.ac.ir/article-1-375-en.htmlcaudal regression syndromespondylocostal dysplasiaspondylothoracic dysplasia
collection DOAJ
language fas
format Article
sources DOAJ
author Hosein Emad Momtaz
Mahmood Jabbari
spellingShingle Hosein Emad Momtaz
Mahmood Jabbari
A Case Report of Jarcho–Levin Syndrome and Caudal Regression Syndrome in A Five Year Old Girl
پزشکی بالینی ابن سینا
caudal regression syndrome
spondylocostal dysplasia
spondylothoracic dysplasia
author_facet Hosein Emad Momtaz
Mahmood Jabbari
author_sort Hosein Emad Momtaz
title A Case Report of Jarcho–Levin Syndrome and Caudal Regression Syndrome in A Five Year Old Girl
title_short A Case Report of Jarcho–Levin Syndrome and Caudal Regression Syndrome in A Five Year Old Girl
title_full A Case Report of Jarcho–Levin Syndrome and Caudal Regression Syndrome in A Five Year Old Girl
title_fullStr A Case Report of Jarcho–Levin Syndrome and Caudal Regression Syndrome in A Five Year Old Girl
title_full_unstemmed A Case Report of Jarcho–Levin Syndrome and Caudal Regression Syndrome in A Five Year Old Girl
title_sort case report of jarcho–levin syndrome and caudal regression syndrome in a five year old girl
publisher Hamadan University of Medical Sciences
series پزشکی بالینی ابن سینا
issn 2588-722X
2588-7238
publishDate 2008-09-01
description Introduction: Jarcho- Levin syndrome and caudal regression syndrome are rare syndromes with clinical and radiologic findings of cervical and thoracic vertebral anomalies with rib deformities (jarcho-levin syndrome) and sacrococcygeal agenesis, lower extremity anomalies, truncated spinal cord and neurogenic bladder (caudal regression syndrome). There are only one report of simultaneous existence of these two syndromes in a dead fetus in literature. Case Report: The case was a 5 year old girl who had history of bilateral hip dysplasia and spastic dipleigia of lower limbs who presented with recurrent urinary tract infections. X - Ray findings was extensive vertebral anomalies such as hemivertebrae, butterfly vertebrae, coccygeal agenesis and rib deformities. MRI findings was termination of spinal cord at low thoracic level, cystic mass of sacral area. Conclusion: This case is a rare simultaneous occurrence of Jarcho-levin and Cauda regression syndrome in a patient and to our best knowledge is reported for the first time in Iran.
topic caudal regression syndrome
spondylocostal dysplasia
spondylothoracic dysplasia
url http://sjh.umsha.ac.ir/article-1-375-en.html
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