Atypical presentation of laryngo‐onycho‐cutaneous syndrome resulting from novel mutations in LAMA3A
- 18 February 2021
- journal article
- research article
- Published by Oxford University Press (OUP) in Clinical and Experimental Dermatology
- Vol. 46 (5), 990-992
- https://doi.org/10.1111/ced.14575
Abstract
No abstract availableKeywords
This publication has 7 references indexed in Scilit:
- A novel mutation in LAMA3A gene in a child with laryngo-onycho-cutaneous syndrome from the Indian subcontinentPublished by Scientific Scholar ,2020
- Using immunofluorescence (antigen) mapping in the diagnosis and classification of epidermolysis bullosa: a first report from IranInternational Journal of Dermatology, 2015
- A new homozygous nonsense mutation inLAMA3Aunderlying laryngo-onycho-cutaneous syndromeBritish Journal of Dermatology, 2013
- The classification of inherited epidermolysis bullosa (EB): Report of the Third International Consensus Meeting on Diagnosis and Classification of EBJournal of the American Academy of Dermatology, 2008
- Granulation tissue in the eyelid margin and conjunctiva in junctional epidermolysis bullosa with features of laryngo-onycho-cutaneous syndromeClinical & Experimental Ophthalmology, 2007
- An unusual N-terminal deletion of the laminin 3a isoform leads to the chronic granulation tissue disorder laryngo-onycho-cutaneous syndromeHuman Molecular Genetics, 2003
- Multisystem disorder of Punjabi children exhibiting spontaneous dermal and submucosal granulation tissue formationClinical Dysmorphology, 1992