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2018, Number 6

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Mul Med 2018; 22 (6)

Jackson-Lawler síndrome. A case report

Ortiz OAM, Blanco SGM, Herrera ÁMJ
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Language: Spanish
References: 0
Page: 1252-1259
PDF size: 281.69 Kb.


Key words:

pachyonychia congenita, palmoplantar keratoderma, steatocystoma multiplex, ectodermal dysplasia.

ABSTRACT

We present a 27-year-old male patient of mixed race, with a history of plantar keratoderma, who attended a specialized in the Celia Sánchez Manduley clinical teaching hospital due to exacerbation of the lesions, accompanied by severe pain when walking; the physical examination revealed the presence of disseminated cystic lesions, nail hypertrophy and alopecia. The case is concluded as a Jackson-Lawler syndrome, highlighting its infrequence in the environment, the impact on the quality of life and the psychological impact generated on the patient and the importance of genetic counseling to them, in order to prevent future generations affected.





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C?MO CITAR (Vancouver)

Mul Med. 2018;22