Background liac arterial fibromuscular dysplasia(FMD)were rarely reported and their demographic,clinical and imaging features have not been precisely described resulting in uncertain therapeutic methods.Methods A lite...Background liac arterial fibromuscular dysplasia(FMD)were rarely reported and their demographic,clinical and imaging features have not been precisely described resulting in uncertain therapeutic methods.Methods A literature review was performed using Pubmed,Web of Science and Embase database.Original articles in English published since 1990 with full-text and detailed demographic,clinical,imaging and therapeutic information regarding iliac arterial FMD were included.展开更多
Ectodermal dysplasia is a rare disease with involvement of teeth,skin and appendages. We report a 2 year old boy presenting with recurrent fever,scarce facial and scalp hair and absence of sweating. Skin and hair biop...Ectodermal dysplasia is a rare disease with involvement of teeth,skin and appendages. We report a 2 year old boy presenting with recurrent fever,scarce facial and scalp hair and absence of sweating. Skin and hair biopsies were suggestive of hypohidrotic ectodermal dysplasia.展开更多
文摘Background liac arterial fibromuscular dysplasia(FMD)were rarely reported and their demographic,clinical and imaging features have not been precisely described resulting in uncertain therapeutic methods.Methods A literature review was performed using Pubmed,Web of Science and Embase database.Original articles in English published since 1990 with full-text and detailed demographic,clinical,imaging and therapeutic information regarding iliac arterial FMD were included.
文摘Ectodermal dysplasia is a rare disease with involvement of teeth,skin and appendages. We report a 2 year old boy presenting with recurrent fever,scarce facial and scalp hair and absence of sweating. Skin and hair biopsies were suggestive of hypohidrotic ectodermal dysplasia.
