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Iranian Journal of Pediatrics. 2011; 21 (1): 121-125
in English | IMEMR | ID: emr-109569

ABSTRACT

Several clinical entities combine ectodermal dysplasia [ED] and cleft lip and/or palate [CL/P]. These disorders have been recognized with a narrow phenotypic spectrum and very similar clinical features. We report a case with a clinical diagnosis of Hay Wells syndrome [ankyloblepharon, ED and CL/P], who is a descendent of a mother with Bowen Armstrong syndrome [ED, CL/P, mental retardation]. Due to the clinical similarities, we suggest that Hay Wells syndrome and Bowen Armstrong syndrome may be the same clinical entity with variable manifestations. This case highlights the difficulties in trying to classify the ED syndromes on clinical features


Subject(s)
Humans , Male , Cleft Lip , Cleft Palate , Eye Abnormalities , Eyelids/abnormalities , Intellectual Disability
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