Lamin A/C gene (LMNA) mutation associated with laminopathy: A rare cause of idiopathic acro-osteolysis-Reference-Cited by-同舟云学术

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Lamin A/C gene (LMNA) mutation associated with laminopathy: A rare cause of idiopathic acro-osteolysis

Published:2019-07 Issue:4 Volume:86 Page:525-527
ISSN:1297-319X
Container-title:Joint Bone Spine
language:en
Short-container-title:Joint Bone Spine

Author:

Lambert Julie-Charlotte,Baudart Pauline,De Sandre-Giovannoli Annachiara,Molin Arnaud^ORCID,Marcelli Christian

Publisher

Elsevier BV

Subject

Rheumatology

Reference9 articles.

1. Sakkas LI. Acro-osteolysis;Botou;Clin Rheumatol,2017

2. A very rare cause of acro-osteolysis: Hajdu-Cheney syndrome;Deprouw;Joint Bone Spine,2015

3. A case of Hajdu-Cheney syndrome associated with psoriatic rheumatism, two causes of acro-osteolysis;Rochoux;Joint Bone Spine,2018

4. Les laminopathies: lipodystrophies, insulino-résistance, syndromes de vieillissement accéléré et les autres;Vigouroux;Annal Endocrinol,2005

5. Mandibuloacral dysplasia;Slimani;Joint Bone Spine,2014

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Familial atrial myopathy in a large multigenerational heart-hand syndrome pedigree carrying an LMNA missense variant in rod 2B domain (p.R335W);Heart Rhythm;2021-11

2. Outcomes of 4 years of molecular genetic diagnosis on a panel of genes involved in premature aging syndromes, including laminopathies and related disorders;Orphanet Journal of Rare Diseases;2019-12

3. Nail changes in acro-osteolysis: A case report and review of the literature;JAAD Case Reports;2019-12

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