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Acta Médica del Centro

ISSN 1995-9494 (Electronic)
Revista del Hospital Clínico Quirúrgico "Arnaldo Milián Castro"
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2012, Number 4

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Acta Med Cent 2012; 6 (4)

Congenital epidermolysis bullosa (Crystal Skin)

Sánchez MLR, García RPP, Viego RME
Full text How to cite this article

Language: Spanish
References: 10
Page:
PDF size: 195.59 Kb.


Key words:

epidermolysis bullosa/genetics, infant, newborn.

ABSTRACT

Epidermolysis bullosa is a skin disorder that is genetically transmitted and that is manifested by the appearance of blisters, ulcers and sores on the skin and mucous membranes with the slightest touch or stroke. The diagnosis is not difficult if the doctor has dermatological experience, but its classification is complex and it is necessary to consider the clinical and genetic aspects, as well as the microscopic and laboratory evaluation. Treatment of this disease is also difficult; and necessary steps needs to be taken in order to protect patients and prevent the occurrence of injuries and complications derived from them. This report presents the case of a newborn white male, diagnosed with epidermolysis bullosa, who was treated at the Teaching Hospital of Placetas.


REFERENCES

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C?MO CITAR (Vancouver)

Acta Med Cent. 2012;6