Hereditary Ectodermal Dysplasia
نویسندگان
چکیده
منابع مشابه
Hereditary Ectodermal Dysplasia - A Case Report
Ectodermal dysplasia is an extremely rare genetic disorder characterized by faulty development of ectodermal structures. The tissues in which the primary defects occur are the skin, hair, nails, exocrine glands, and teeth. It usually affects the males and females are the carriers. The clinical features include sparse hair, abnormal or missing teeth, and inability to sweat due to lack of sweat g...
متن کاملHereditary Ectodermal Dysplasia : A Case Report
Virender Kumar, Lalit Kumar Dr HSJ Institute of Dental Sciences and Hospital Panjab University Chandigarh, India Ectodermal dysplasia (ED) is a hereditary disease characterized by anomalies in the structures of ectodermal origin. The disease affects skin, saliva, sebaceous and sweat glands (anhidrosis or hypohidrosis), hair (atrichosis or hypotrichosis), nail and teeth (anodontia or hypodontia)...
متن کاملHereditary ectodermal dysplasia: a case report.
Hereditary ectodermal dysplasia is an inherited disorder involving skin, hair, nails and teeth. Two main clinical forms have been described--hypohidrotic type and hidrotic type. A case of ectodermal dysplasia with absence of hypohidrosis and defective nails has been reported. The importance of early prosthetic management has been discussed.
متن کاملHypodontia and microdontia associated with hereditary ectodermal dysplasia.
Hypodontia and associated conditions like Hereditary Ectodermal Dysplasia (HED) and microdontia markedly influence on physical, functional and psychosocial maturation of the affected individuals. Thorough evaluation, proper counseling and careful treatment planning employing a multidisciplinary approach are keys to a successful, long-term management. This case report describes the prosthodontic...
متن کاملHereditary ectodermal dysplasia, olivopontocerebellar degeneration, short stature, and hypogonadism.
Two teenaged children born of normal parents in a consanguineous family had evidence of abnormal neurological, endocrine, and ectodermal development. They had mental retardation, hearing loss, ocular dysmetria, hyperreflexia, and ataxia consistent with olivopontocerebellar degeneration. They had hypogonadotrophic hypogonadism and extremely short stature despite normal serum growth hormone and s...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Proceedings of the Royal Society of Medicine
سال: 1964
ISSN: 0035-9157
DOI: 10.1177/003591576405700218