Literature DB >> 19050401

Sudden death in spondylo-meta-epiphyseal dysplasia, short limb-abnormal calcification type.

Cristina Dias1, Robyn Cairns, Millan S Patel.   

Abstract

The spondylo-meta-epiphyseal dysplasias are an expanding group of skeletal dysplasias with specific features differentiating each subtype. We review the precocious carpal mineralization, unique metacarpal shape, triangular distal phalanges and mushroom cloud-shaped proximal phalanges present at an early age in spondylo-meta-epiphyseal dysplasia, short limb-abnormal calcification type (SMED SL-AC) and report two patients with clinical and radiographic features consistent with SMED SL-AC, who died suddenly because of spinal cord compression. The patients presented are female siblings, providing further evidence for autosomal recessive inheritance. Cervical cord compression is found in half of reported patients and is the major cause of mortality. SMED SL-AC should be added to the list of genetic causes of sudden death. Radiological features in the hand may be used in the first few years of life to support an early diagnosis and thus allow for prevention of premature demise.

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Year:  2009        PMID: 19050401     DOI: 10.1097/MCD.0b013e3283186907

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


  7 in total

1.  Spondyloepimetaphyseal dysplasia, short limb-abnormal calcifications type: progressive radiological findings from fetal age to adolescence.

Authors:  Katya Rozovsky; Jacob Sosna; Martine Le Merrer; Natalia Simanovsky; Benjamin Z Koplewitz; Jacob Bar-Ziv; Valerie Cormier-Daire; Annick Raas-Rothschild
Journal:  Pediatr Radiol       Date:  2011-08-05

2.  Further expansion of the mutational spectrum of spondylo-meta-epiphyseal dysplasia with abnormal calcification.

Authors:  Gizem Ürel-Demir; Pelin Ozlem Simsek-Kiper; Özlem Akgün-Doğan; Rahşan Göçmen; Zheng Wang; Naomichi Matsumoto; Noriko Miyake; Gülen Eda Utine; Gen Nishimura; Shiro Ikegawa; Koray Boduroglu
Journal:  J Hum Genet       Date:  2018-06-08       Impact factor: 3.172

3.  Report of a Novel Homozygous Nonsense DDR2 Mutation in an Indian Adult Male with Spondylo-meta-epiphyseal Dysplasia, Short Limb-Abnormal Calcification Type.

Authors:  Neerja Gupta; Alec Reginald Errol Correa; Manisha Jana; Madhulika Kabra
Journal:  J Pediatr Genet       Date:  2019-03-12

4.  Spondylometaepiphyseal Dysplasia Short Limb-Abnormal Calcification Type in Turkish Patients Reveals a Novel Mutation and New Features.

Authors:  Elif Yilmaz Gulec; Bassam R Ali; Anne John; Beyhan Tuysuz
Journal:  Mol Syndromol       Date:  2021-09-28

5.  Trafficking defects and loss of ligand binding are the underlying causes of all reported DDR2 missense mutations found in SMED-SL patients.

Authors:  Bassam R Ali; Huifang Xu; Nadia A Akawi; Anne John; Noushad S Karuvantevida; Ruth Langer; Lihadh Al-Gazali; Birgit Leitinger
Journal:  Hum Mol Genet       Date:  2010-03-10       Impact factor: 6.150

6.  Identification of a novel homozygous mutation in the DDR2 gene from a patient with spondylo-meta-epiphyseal dysplasia by whole exome sequencing.

Authors:  Masoud Heidari; Morteza Soleyman-Nejad; Alireza Isazadeh; Mohammad Hossein Taskiri; Manzar Bolhassani; Nahid Sadighi; Zahra Shiri; Zahra Karimi; Mansour Heidari
Journal:  Iran J Basic Med Sci       Date:  2021-02       Impact factor: 2.699

7.  A novel mutation in DDR2 causing spondylo-meta-epiphyseal dysplasia with short limbs and abnormal calcifications (SMED-SL) results in defective intra-cellular trafficking.

Authors:  Adila Al-Kindi; Praseetha Kizhakkedath; Huifang Xu; Anne John; Abeer Al Sayegh; Anuradha Ganesh; Maha Al-Awadi; Lamya Al-Anbouri; Lihadh Al-Gazali; Birgit Leitinger; Bassam R Ali
Journal:  BMC Med Genet       Date:  2014-04-11       Impact factor: 2.103

  7 in total

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