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ectodermal dysplasia/palavik

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Leht 1 alates 73 tulemused

Recurrent fever and lack of tooth buds. a case of ectodermal dysplasia in a 9 months old boy.

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We present the case of a 9 months old boy with an X-linked form of anhidrotic (hypohidrotic) ectodermal dysplasia. Several chest X-rays had been performed to rule out pneumonia because of recurrent episodes of high fever. The child's lack of tooth buds (hypodontia), which could be encountered on the
To evaluate exertional overheating and the impact of physical exercise on individuals with hypohidrotic ectodermal dysplasia (HED) and to assess protective effects of cooling devices, 13 boys and male adolescents with X-linked HED (XLHED) and age-matched healthy male controls were studied during

[Hypohidrotic ectodermal dysplasia as the cause of recurrent hyperthermia in a young infant].

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Fever--the most frequent symptom of diseases in children--points diagnostically to an infection. We report on a child who presented with recurrent high fever of unknown origin. Infectious diseases could be excluded. During a general medical checkup the results of repeated pilocarpine iontophoresis

[Anhydrotic ectodermal dysplasia as cause of recurrent hyperthermia in a 5 month old infant].

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The X-linked anhydrotic ectodermal dysplasia is a rare disease in which defects in development of ectodermal derivatives are observed. This syndrome is clinically characterized by total or partial anodontia, characteristic physionomy and absent or reduced sweating. Recurrent fever was a clue to the

[Anhidrotic ectodermal dysplasia as a cause of fever of undetermined origin (presentation of a case)].

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The authors present the case of a patient hospitalized with the diagnosis of "fever of undetermined origin" (FUO) in whom the physical examination and laboratory tests (including a skin biopsy) showed that the child had anhidrotic ectodermal dysplasia. We study the differential diagnosis, the

[Hypohidrotic ectodermal dysplasia: A cause of fever of unknown origin].

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The term ectodermal dysplasias includes many disorders that share some clinical features such as involvement of one or several ectodermal structures and congenital origin. Currently, 154 different types divided into 11 clinical subgroups (Freire Maia classification 1994) have been described. The

A case of anhidrotic ectodermal dysplasia presenting with pyrexia, atopic eczema, and food allergy.

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Anhidrotic ectodermal dysplasia (AED) is a rare hereditary disorder with a triad of sparse hair, dental hypoplasia, and anhidrosis. Here we report a case of AED with food allergy and atopic eczema. The patient was a 11-month-old boy admitted to our hospital with pyrexia for 2 weeks. He presented

Fever and hypotrichosis in a newborn. Anhidrotic ectodermal dysplasia (AED).

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Anhidrotic ectodermal dysplasia. An unusual case of pyrexia in the newborn.

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[Anhydrotic ectodermal dysplasia: un uncommon cause of unexplained fever in infants].

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Ectodermal dysplasia presenting as fever of unknown origin.

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Anhidrotic ectodermal dysplasia; fever in a neonate.

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A rare cause of fever of unknown origin: hypohidrotic ectodermal dysplasia with a splice site mutation.

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Anhidrotic ectodermal dysplasia presenting as a pyrexia of undertermined origin in the neonatal period.

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