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Scholars Journal of Medical Case Reports | Volume-2 | Issue-06
A Rare Case Report of Anhidrotic Ectodermal Dysplasia in a Newborn
Jyothsna B, S. Pratap Rao, Khurram Ali, Ravi Kiran J, Shilpa D, Narayan Reddy U
Published: June 30, 2014 | 103 60
DOI: 10.36347/sjmcr.2014.v02i06.018
Pages: 408-410
Ectodermal Dysplasias are a heritable group of disorders characterized by faulty development of two or more tissues derived from embryonic ectoderm. This disorder primarily involves skin, hair, nails, teeth and eccrine glands. The disease is usually diagnosed in late infancy and childhood but early diagnosis in a newborn baby tends to have good prognosis. We report a rare case of Anhidrotic Ectodermal Dysplasia in a 26 day old Newborn baby presenting with recurrent episodes of fever, hypotrichosis and anhydrosis.