Unrecognized fracture both bones leg with hypertrophic callus in a child with hypohidrotic ectodermal dysplasia
نویسندگان
چکیده
منابع مشابه
Hypohidrotic ectodermal dysplasia.
X linked hypohidrotic ectodermal dysplasia was studied in the dentition of both affected males and carrier females. Hypodontia was more severe in males than females and there were differences in the pattern of tooth absence between the sexes. Abnormal crown form, with the maximum diameter of the teeth being apically displaced, was noted particulady in the anterior teeth. Taurodontism was common...
متن کاملHypohidrotic ectodermal dysplasia: a clinical case with a longitudinal approach.
AIM This paper describes a clinical case of a male with hypohidrotic ectodermal dysplasia submitted to rehabilitation and occlusal dental interventions with follow-up from 3 to 14 years of age. BACKGROUND Due to the severe effects on function and esthetics, the clinical manifestations of ectodermal dysplasia exert a negative impact on quality of life. However, oral rehabilitation in childhood...
متن کاملOral rehabilitation with implant-supported overdenture in a child with hypohidrotic ectodermal dysplasia
suffering from severe hypodontia, however, conventional prostheses are inadequate due to lack of retention and instability. The replacement of teeth by implants is usually restricted to patients with completed craniofacial growth; however, implants can be used as abutments for overdentures. This study reports a 9-year follow-up case of a child affected with X-linked hypohidrotic ectodermal dysp...
متن کاملGenetic counselling of a male patient with hypohidrotic ectodermal dysplasia
Hypohidrotic ectodermal dysplasias (HED) are characterized by abnormal morphogenesis of epidermis and epidermal appendages. They may be inherited in an autosomal dominant, autosomal recessive or X-linked recessive manner. The most common type shows Xlinked inheritance, and males.are usually more severely affected than females. In a male infant who was treated in our department, the diagnosis of...
متن کاملSubtotal amelia in a child with autosomal recessive hypohidrotic ectodermal dysplasia.
We report an inbred Tunisian family, in which the proband manifested signs of hypohidrotic ectodermal dysplasia, subtotal amelia, scoliosis and left renal agenesis. Two other family members had the full clinical criteria of hypohidrotic ectodermal dysplasia, characterized by deficient sweat glands, hypodontia, hypoplasia of the mucous glands, and fine hair. Nine family subjects had variable cli...
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ژورنال
عنوان ژورنال: Orthopaedic Surgery
سال: 2011
ISSN: 1757-7853
DOI: 10.1111/j.1757-7861.2010.00111.x