Publication: Dyskeratosis congenita: a rare case report Authors
| creativeworkseries.issn | ISSN 1990-7974 eISSN 1990-7982 | |
| dc.contributor.author | Roy, Banasree | |
| dc.contributor.author | Mondal, Gobinda | |
| dc.contributor.author | Paul, Dilip Kumar | |
| dc.contributor.author | Kalam, Abul | |
| dc.contributor.author | Basu, Kausambi | |
| dc.date.accessioned | 2026-05-22T10:37:06Z | |
| dc.date.available | 2026-05-22T10:37:06Z | |
| dc.date.issued | 2013 | |
| dc.description | Banasree Roy R.M.O. cum Clinical Tutor, Dr. B.C.Roy Postgraduate Institute of Paediatric Sciences, Kolkata Gobinda Mondal Assistant Professor, Department of Paediatric Medicine, Burdwan Medical College, West Bengal Dilip Kumar Paul Medical Superintendent cum Vice Principal, Dr. B.C. Roy Postgraduate Institute of Paediatric Sciences, Kolkata Abul Kalam Assistant Professor, Dr. B.C.Roy Postgraduate Institute of Paediatric Sciences, Kolkata 70054, West Bengal Kausambi Basu Senior Resident, Dr. B.C.Roy Postgraduate Institute of Paediatric Sciences, Kolkata 70054, West Bengal | |
| dc.description.abstract | Abstract: Dyskeratosis congenita is a rare congenital disorder affecting mainly the integumentary system. It is a progressive disease with involvement of bone marrow. A triad of hyperpigmentation, nail dystrophy and leucoplakia are characteristic of this disease. | |
| dc.identifier | https://doi.org/10.3126/jnps.v33i3.8166 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.14572/6218 | |
| dc.language.iso | en_US | |
| dc.publisher | Nepal Paediatric Society (JNPS) | |
| dc.subject | Hyperpigmentation | |
| dc.subject | nail dystrophy | |
| dc.subject | leucoplakia | |
| dc.title | Dyskeratosis congenita: a rare case report Authors | |
| dc.type | Article | |
| dspace.entity.type | Publication | |
| local.article.type | Case Report | |
| oaire.citation.endPage | 226 | |
| oaire.citation.startPage | 223 | |
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