Literature DB >> 9784647

Congenital rapidly fatal form of nemaline myopathy with fetal hydrops and arthrogryposis. A case report and review.

D Vardon1, C Chau, S Sigodi, D Figarella-Branger, L Boubli.   

Abstract

A new lethal case of nemaline myopathy is reported. The diagnosis was made by postmortem muscle biopsy. The child died before his first day of life. This is one of the very rare cases of nemaline myopathy with severe antenatal ultrasonographic signs: fetal hydrops and arthrogryposis. In a review of the literature other cases of the congenital rapidly fatal form are found, some of them with clinical decrease of fetal movements but only few authors report ultrasonographic signs. The diagnostic, histopathogenic, genetic and evolutive aspects of this heterogeneous disorder are analyzed. This congenital nonprogressive myopathy is not as benign as previously thought and may be an etiology of the lethal form of arthrogryposis multiplex congenita. The existence of ultrasonographic antenatal signs seems to be a factor of poor prognosis. In spite of recent genetic discoveries, there is at present no specific antenatal diagnosis. Consequently, muscle biopsy in lethal cases is very important to allow a genetic counselling; however, in utero fetal biopsy has never been performed in such cases.

Entities:  

Mesh:

Year:  1998        PMID: 9784647     DOI: 10.1159/000020847

Source DB:  PubMed          Journal:  Fetal Diagn Ther        ISSN: 1015-3837            Impact factor:   2.587


  4 in total

1.  Identification of embryonic lethal genes in humans by autozygosity mapping and exome sequencing in consanguineous families.

Authors:  Hanan E Shamseldin; Maha Tulbah; Wesam Kurdi; Maha Nemer; Nada Alsahan; Elham Al Mardawi; Ola Khalifa; Amal Hashem; Ahmed Kurdi; Zainab Babay; Dalal K Bubshait; Niema Ibrahim; Firdous Abdulwahab; Zuhair Rahbeeni; Mais Hashem; Fowzan S Alkuraya
Journal:  Genome Biol       Date:  2015-06-03       Impact factor: 13.583

2.  The KLHL40 c.1516A>C is a Chinese-specific founder mutation causing nemaline myopathy 8: Report of six patients with pre- and postnatal phenotypes.

Authors:  Kit San Yeung; Florrie N Y Yu; Cheuk Wing Fung; Sheila Wong; Hencher H C Lee; Sharon T H Fung; Genevieve P G Fung; Kwok Yin Leung; Wai Hang Chung; Yun Ting Lee; Vivian K S Ng; Mullin H C Yu; Jasmine L F Fung; Mandy H Y Tsang; Kelvin Y K Chan; Sophelia H S Chan; Anita S Y Kan; Brian H Y Chung
Journal:  Mol Genet Genomic Med       Date:  2020-04-30       Impact factor: 2.183

3.  Compound Heterozygosity for Novel Truncating Variants in the LMOD3 Gene as the Cause of Polyhydramnios in Two Successive Fetuses.

Authors:  Ye Wang; Caixia Zhu; Liu Du; Qiaoer Li; Mei-Fang Lin; Claude Férec; David N Cooper; Jian-Min Chen; Yi Zhou
Journal:  Front Genet       Date:  2019-09-13       Impact factor: 4.599

4.  Case Report: Prenatal Diagnosis of Nemaline Myopathy.

Authors:  Dongmei Liu; Jiali Yu; Xin Wang; Yang Yang; Li Yu; Shi Zeng; Ming Zhang; Ganqiong Xu
Journal:  Front Pediatr       Date:  2022-07-19       Impact factor: 3.569

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.