Hydrotic or Hypohydrotic Ectodermal Dysplasia: Diagnostic Dilemmas (Case Report)
نویسندگان
چکیده
Ectodermal dysplasia includes a large group of syndromes that are clinically and genetically heterogeneous, and are identified by anomalies in structures of ectodermalorigin, and can present with disorders in such structures as hair, nail, teeth, sweat glands, sebaceous glands and conjunctiva and nervous system (Ramesh et al., 2010). This syndrome was first reported by Charles Darwin (1860) (Mirkarimi et al., 2010).
منابع مشابه
Multidisciplinary management of hypohydrotic ectodermal dysplasia – a case report
Hypohydrotic ectodermal dysplasia is a hereditary disorder, which affects ectodermal derivatives. It manifests several abnormalities of the teeth, and is commonly inherited through female carriers. This case report presents a patient with compromised esthetics and function. A multidisciplinary approach was planned involving an oral pathologist, endodontist, orthodontist and a prosthodontist.
متن کاملDental Management of Ectodermal Dysplasia Syndrome at an Early Age: A Case Report
Objectives: Ectodermal dysplasia (ED) is a relatively common sex-linked dermatitis characterized by congenital dysplasia of one or more ectodermal structures and their accessory appendages. Common manifestations include fragile skin and nails, defective teeth and salivary glands, frontal bossing with prominent supra orbital ridges, nasal bridge depression and protuberant lips. Teeth are often f...
متن کاملEctodermal Dysplasia Syndrome withOrthodontic Treatment and Oral Finds: A CaseReport
Ectodermal dysplasia, which affects ectodemal derivatives, currently is an X-linked recessive inheritary hypohydrotic ectodermal dysplasia. Patients with ectodermal dysplasia usually characterized by congenital teeth loss, abnormal teeth and inherited through female carriers. In this case report, we present a 5 years old boy of China ethnicity with mandibular anodontia, a rare dental dysplasia ...
متن کاملHypohydrotic Ectodermal Dysplasia -a Case Report
Ectodermal dysplasia is a rare hereditary disorder. Its Hypohidrotic (HED) variant is also known as ChirstSiemens-Touraine syndrome. It is inherited as an Xlinked trait. Such Patients are characterized by the clinical manifestations of Hypodontia, Hypotrichosis, Hypohidrosis and a highly characteristic facial physiognomy. This article, reports a typical case of Hypohidrotic Ectodermal Dysplasia...
متن کاملSolitary eccrine syringofibroadenoma: a case report showing papillary tubular adenoma-like features
Eccrine syringofibroadenoma (ESFA) is a rare tumor originated from eccrine ductal portion [1,2]. Clinically, ESFA presents a solitary papule, nodule or plaque to multiple lesions. Cases with multiple papular or macular lesions have been often associated with hereditary ectodermal dysplasia [3]. Recent findings have classified ESFA into several groups including, solitary ESFA, multiple ESFA with...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
عنوان ژورنال:
دوره شماره
صفحات -
تاریخ انتشار 2002