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ISSN 1029-3019 (Electronic)

2022, Number 01

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MediSan 2022; 26 (01)

Arlekin ichthyosis in a newborn baby

Leyva PYE, Querol BN, González RM

Language: Spanish
References: 10
Page: 133-140
PDF size: 649.80 Kb.


ABSTRACT

The case report of a newborn baby, product of an eutocic childbirth, at term and normal weight, is described. He was assisted in Barrillas Distrital Hospital, belonging to the rural area of the Huehuetenango Department in Guatemala due to big and thick flakes disseminated in the skin when being born, as well as eversion of eyelids and lips. Arlekin ichthyosis was diagnosed, reason why he was admitted to the Neonates Care Unit of this center. The clinical course was unfavorable, with persistence of complications, such as serious sepsis and hydroelectrolitic disorders, in spite of the medical treatment, reason why he died after 6 days of being born and same period of hospitalization.


REFERENCES

  1. Wright T. The genodermatosis. UpToDate [citado 03/11/2020]. Disponible en: https://www.uptodate.com/contents/the-genodermatoses-an-overview

  2. Pandey R. Congenital Icthyosis: A case report. Clin Res Trials. 2017 [03/11/2020];3(2):1-3. Disponible en: https://www.oatext.com/Congenital-icthyosis-A-case-report.php

  3. Paez E, Tobia S, Colmenarez V, Herrera K, Duarte JM, Vivas SC. Ictiosis lamelar autosómica recesiva: revisión de la literatura y caso clínico. Rev. Argent. Dermatol. 2020 [citado 24/04/2020];101(1). Disponible en: https://rad-online.org.ar/2020/05/19/ictiosis-lamelar-autosomica-recesiva-revision-de-la-literatura-y-caso-clinico/

  4. Ugezu CH, Mazumdar A, Dunn E, Das A. Harlequin Ichthyosis. A case Report. Ir Med J. 2017 [citado 18/09/2020];110(7). Disponible en: https://pubmed.ncbi.nlm.nih.gov/29341518/

  5. Carvajalino F, Peña L. Ictiosis arlequín, una genodermatosis devastadora. Repert Med Cir. 2018 [citado 24/04/2020];27(1). Disponible en https://www.fucsalud.edu.co/sites/default/files/2018-07/Rep-caso-Ictiosis-arlequin.pdf

  6. Navarro SJ, Molina Barrios SJ. Caso de ictiosis laminar en honduras. Rev Cient Cienc Méd. 2018 [citado 03/11/2020];21(2):73-4. Disponible en: http://www.scielo.org.bo/scielo.php?script=sci_arttext&pid=S1817-74332018000200013

  7. El-Sayed N, Seifeldin NS, Gobriol CKT. High frecuency of primary hereditaryichthyosis in the North-East Region of Cairo, Egypt. Postepy Dermatol Alergol. 2018 [citado 18/09/2020];35(2). Disponible en: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5949546/

  8. Leone de Moraes ET, Souza Freire MH, Rocha F, Linha Secco I, Costa T, Queiroz Afonso R. Nursing care for a newborn with Lamellar Ichthyosis: a case study in a neonatal unit. Rev Esc Enferm USP. 2019 [citado 15/01/2020];53. Disponible en: https://pubmed.ncbi.nlm.nih.gov/31800813/

  9. Sheth JS, Bhavsar R, Patel D, Joshi A, Seth FJ. Harlequin ichthyosis due to novel splice site mutation in the ABCA12 gene: postnatal to prenatal diagnosis. Int J Dermatol. 2018 [citado 24/04/2020];57(4). Disponible en: https://pubmed.ncbi.nlm.nih.gov/29377090/

  10. Glick J, Craiglow B, Choate K, Kato H, Fleming R, Siegfried E, et al. Glick Improved Management of Harlequin Ichthyosis with Advances in Neonatal Intensive Care. Pediatrics. 2017 [citado 18/09/2020]; 139 (1). Disponible en: https://pubmed.ncbi.nlm.nih.gov/27999114/




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