A Case Study of Pachyonychia Congenita in Bangladesh

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  •   Zahed Parvez

  •   Samina Akter

Abstract

In 1906 Jadassohn and Lewandowsky described a rare genodermatoses and named it pachyonychia congenita. Pachy means thick. It is a group of genodermatoses involving keratin mutation with thickened nails and variable associated findings. Pachyonychia congenita is a rare disease having four types. However, type 1 and type 2 can be considered common among them. It can often mimic with fungal infection as nail hyperkeratosis can occur in both.


Keywords: Hyperkeratosis, Mutation, Pachyonychia congenita, Rare

References

Acta Derm Venereol, 55 (1975), pp. 387-394.

A letter from Mr St. George Ash, Sec. of the Dublin Society, to one of the Secretaries of the Royal Society: Concerning a girl in Ireland, who has several horns growing on her body. Phil Trans Rl Soc London, 15 (1685), pp. 1202-1204.

Benjamin et al., 1987. B. Benjamin, D.S. Parsons, H.F. Molloy, Pachyonychia congenita with laryngeal involvement, Int J Pediatr Otorhinolaryngol, 13 (1987), pp. 205-209.

J. Bondeson, Pachyonychia congenita. A historical note, Am J Dermatopathol, 15 (1993), pp. 594-599.

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How to Cite
Parvez, Z., & Akter, S. (2021). A Case Study of Pachyonychia Congenita in Bangladesh. European Journal of Medical and Health Sciences, 3(3), 16-17. https://doi.org/10.24018/ejmed.2021.3.3.822