An infant with X‐linked anhidrotic ectodermal dysplasia with immunodeficiency presenting with Pneumocystis pneumonia: A case report.

Autor:	Toyohara, Miwako, Kajiho, Yuko, Toyofuku, Etsushi, Takahashi, Chie, Owada, Keiho, Kanda, Shoichiro, Harita, Yutaka, Ohnishi, Hidenori, Wada, Taizo, Imai, Kohsuke, Kanegane, Hirokazu, Morio, Tomohiro, Oka, Akira
Předmět:	ECTODERMAL dysplasia PNEUMOCYSTIS pneumonia INFANTS PRIMARY immunodeficiency diseases GENETIC counseling IMMUNODEFICIENCY
Zdroj:	Clinical Case Reports; Nov2021, Vol. 9 Issue 11, p1-5, 5p
Abstrakt:	Pneumocystis jirovecii pneumonia associated with primary immunodeficiency should be considered in infants with slowly progressing cyanosis, even without fever or respiratory symptoms. Genetic counseling is crucial for incontinentia pigmenti families in advance of pregnancy because lethal infections can occur before the diagnosis of X‐linked anhidrotic ectodermal dysplasia with immunodeficiency. [ABSTRACT FROM AUTHOR]
Databáze:	Complementary Index
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