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Collodion Baby and its Further Development


Authors: B. Pinková 1;  L. Fajkusová 2;  R. Borská 2;  H. Bučková 1
Authors‘ workplace: Dětské kožní oddělení Pediatrické kliniky, LF MU a FN Brno, vedoucí pracoviště MUDr. Blanka Pinková 1;  Centrum molekulární biologie a genové terapie IHOK FN Brno a LF MU v Brně, vedoucí pracoviště prof. RNDr. Šárka Pospíšilová, Ph. D. 2
Published in: Čes-slov Derm, 95, 2020, No. 5, p. 159-165
Category: Reviews (Continuing Medical Education)

Overview

Collodion baby (CB) is a specific phenotype of a genodermatosis, in which a newborn is born with parchment-like membrane on the skin. Clinical manifestations of the individual types of ichtyoses that develop from CB change with patient’s age. The diagnostic method of choice nowadays is molecular analysis, which also enables complex genetic counseling and genetic prevention. Patients should be reffered to specialized centers where laboratory facilities are available, and where multidisciplinary care provided by neonatologists, pediatricians, dermatologists and other specialists is possible.

Keywords:

collodion baby – ectropium – eclabium – diagnostics – DNA molecular analysis – therapy


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