Christ Siemen Syndrome - a Report of Two Cases

Abstract

Ectodermal Dysplasia (ED) is a rare hereditary disorder which is characterized by triad of signs comprising sparse hair, abnormal or missing teeth and inability to sweat. This article comprises of 2 such cases one of a 5 year old child with hypohydroic ectodermal dysplasia and a 15 year old female patient of clustons syndrome. This paper also highlights about history, clinical features, differential diagnosis and treatment options of such patients.