Hereditary Madelung's disease
Author:
Affiliation:
1. Department of Plastic Surgery, Mount Vernon Hospital, Northwood, Middlesex, UK
Publisher
SAGE Publications
Subject
General Medicine
Link
http://journals.sagepub.com/doi/pdf/10.1177/014107680009300411
Reference6 articles.
1. Symmetric Lipomatoses in Female Patients
2. Mitochondrial dysfunction with myoclonus epilepsy and ragged-red fibers point mutation in nerve, muscle, and adipose tissue of a patient with multiple isymmetric lipomatosis
3. Oropharyngeale Fetthernie bei Madelunq'schem Fetthals als seltene Ursache einer akuten Dysphagie*
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1. Analysis of Madelung disease based on sc-RNA sequencing: A case report and literature review;Molecular Immunology;2023-05
2. Surgical Treatment of Madelung’s Disease: Case Report and Literature Review;Indian Journal of Surgery;2022-11-14
3. Neuropatía óptica hereditaria y síndromes sistémicos asociados como resultado del solapamiento de 2 mutaciones mitocondriales;Neurología;2021-07
4. Hereditary optic neuropathy and associated systemic diseases due to 2 overlapping mitochondrial mutations;Neurología (English Edition);2021-04
5. Cbl Proto-Oncogene B (CBLB) c.197A>T Mutation Induces Mild Metabolic Dysfunction in Partial Type I Multiple Symmetric Lipomatosis (MSL);Diabetes, Metabolic Syndrome and Obesity: Targets and Therapy;2020-10
Cbl Proto-Oncogene B (CBLB) c.197A>T Mutation Induces Mild Metabolic Dysfunction in Partial Type I Multiple Symmetric Lipomatosis (MSL)
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