Clinical heterogeneity in epidermolysis bullosa simplex with plectin (PLEC) mutations—A study of six unrelated families from India. Issue 8 (17th May 2022)

• Record Type: Journal Article
• Authors: Vishwanathan, Gurudatta Baraka; Srinivasa, Manoj; Batrani, Meenakshi; Kubba, Asha; Ghosh, Suparna; Gupta, Divya; Jayashankar, Charitha; Rai, Abhigna; Jangond, Ajith; Inamadar, Arun; Hiremagalore, Ravi
• Is Part Of: American journal of medical genetics. Volume 188:Issue 8(2022)
• Page Start: 2454
• Page End: 2459
• Publication Date: 2022-05-17
• Subjects: antigen mapping -- EBS -- intermediate filaments -- muscular dystrophy -- plectin; Medical genetics -- Periodicals; 616.14205
• DOI: 10.1002/ajmg.a.62781
• Languages: English
• ISSNs: 1552-4825

Abstract

Abstract: Epidermolysis bullosa simplex (EBS) with plectin mutations is a very rare subtype of EB usually associated with pyloric atresia (PA) or muscular dystrophy (MD). We report six unrelated children between ages 4 and 14 years from India with varied clinical manifestations. Only one had PA, and none has developed MD to date. All except the one with PA presented with early onset blistering along with laryngeal involvement in the form of hoarseness of voice and nail involvement. Patient with PA presented with aplasia cutis and died in the first week. Two patients had predominantly respiratory and gastrointestinal involvement with varying severity while two had features of myasthenic syndrome but no limb‐girdle involvement and one patient phenocopied laryngo‐onycho‐cutaneous (LOC) syndrome. Using whole‐exome sequencing, we identified novel mutations in PLEC . Histopathological analysis (Immunofluorescence antigen mapping) showed absence of staining to plectin antibodies. Our observations propose to append a phenotype of EBS, hoarseness of voice and nail dystrophy or LOC‐like phenotype with plectin mutations. Long‐term follow up is necessary to monitor for the development of muscular dystrophy.