Results 141 to 150 of about 737 (185)
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Eccrine syringofibroadenomatosis associated with hidrotic ectodermal dysplasia
British Journal of Dermatology, 1998Eccrine syringofibroadenoma (ES) is generally regarded as a solitary benign adnexal neoplasm of the skin. Recently, the epithelial and stromal changes of this lesion have been recognized as being a reaction pattern in certain settings. We describe two individuals in whom this process was a manifestation of hidrotic ectodermal dysplasia.
E L, Simpson +2 more
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Hypotrichosis and nail dysplasia: A novel hidrotic ectodermal dysplasia
Australasian Journal of Dermatology, 2004SUMMARYWe report a unique isolated hair and nail ectodermal dysplasia in a 3‐year‐old girl. Clinical examination revealed short, sparse scalp hair, absent eyebrows, short eyelashes and nail dystrophy in all digits. Nail changes included shortened nail plate with distal onycholysis and loss of the cuticle. Sweating and teeth were normal. Development was
Shannon, Harrison, Rodney, Sinclair
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Hidrotic Ectodermal Dysplasia: A Clinical and Ultrastructural Observation
Dermatology, 1988Hidrotic ectodermal dysplasia (HED) was observed in a 49-year-old Japanese man. His clinical signs included alopecia, dystrophic nails and palmoplantar keratoderma, but his teeth, facial appearance and sweating were normal. In his family, 9 members in 5 generations were affected, suggesting that the disorder has an autosomal dominant mode of ...
Y, Ando +4 more
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Hidrotic Ectodermal Dysplasias
1987Ectodermal dysplasias (EDs) represent a large heterogeneous group of different malformations of cutaneous appendages. The lowest common denominator of these EDs is disorders of at least two ectodermal differentiation products [7, 31]: (1) hair anomaly, (2) dental anomaly, (3) onychodysplasia, or (4) sweat gland anomaly.
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[Hidrotic ectodermal dysplasia].
Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete, 1976This paper reports a family with typical features of hidrotic ectodermal dysplasia (h.e.d.). Although some members of the family showed phenotypical similarities to anhidrotic ectodermal dysplasia, there is no doubt about the classification of this disorder into hidrotic ectodermal dysplasia because of its manifest symptomatology (hypo- and ...
P, Altmeyer, I, Schindera
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New form of hidrotic ectodermal dysplasia in a Lebanese family
American Journal of Medical Genetics, 1998We report a sister and brother born to consanguineous parents presenting with severe hypodontia, fine hair, and onychodysplasia. Five other relatives are similarly affected. The comparison with other ectodermal dysplasias is presented and discussed. The possibility of a new autosomal recessive form of ectodermal dysplasia is raised.
A, Mégarbané +3 more
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Hidrotic Ectodermal Dysplasia With Diffuse Eccrine Syringofibroadenomatosis
Archives of Dermatology, 1989To the Editor.— Hidrotic ectodermal dysplasia (HED) is an uncommon autosomal-dominant disorder characterized by palmoplantar hyperkeratosis, dystrophy of the nails, and defects of the hair. It is sometimes associated with a large constellation of other abnormalities. 1 In this report, we describe a case of HED in a patient with numerous papules on the
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A man, a syndrome, a gene: Clouston's hidrotic ectodermal dysplasia (HED)
American Journal of Medical Genetics, 2001This paper presents a biographical sketch of Dr. H. R. Clouston, whose eponym is attached to a type of hidrotic ectodermal dystrophy, and a brief account of the mapping of the gene and its identification as the connexin gene, GJB6.
F C, Fraser, V M, Der Kaloustian
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[Hidrotic ectodermal dysplasia syndrome--trichooculodermatovertebral syndrome].
Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete, 1992We report on a 23-year-old women suffering from a hidrotic ectodermal dysplasia with baldness, xerodermia, kyphosis of the chest, hypopigmented mamillae, disturbances of the menstrual cycle, dysphonia and keratitis punctata superficialis recidivans. The complex condition is classified as a tricho-oculo-dermo-vertebral syndrome.
U, Wollina, H, Roth, H, Schaarschmidt
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[Primary anodontia in X-linked hidrotic ectodermal dysplasia].
Stomatologiia, 1998Nine patients with congenital deciduous and permanent adentia are described for the first time in Russia. Published reports are reviewed and recommendations on the DNA and prenatal diagnosis offered, which permit detecting women at a high risk of giving birth to handicapped children.
Iu A, Beliakov +3 more
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