Results 191 to 200 of about 34,736 (238)
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Dermatology, 1979
Description of a patient presenting an hidrotic ectodermal dysplasia. Clinical signs were hypotrichosis, dystrophic nails, palmoplantar keratoderma, absence of teeth and hyperhidrosis.
G E, Pierard, D, Van Neste, B, Letot
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Description of a patient presenting an hidrotic ectodermal dysplasia. Clinical signs were hypotrichosis, dystrophic nails, palmoplantar keratoderma, absence of teeth and hyperhidrosis.
G E, Pierard, D, Van Neste, B, Letot
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Acta Paediatrica, 1952
SummaryTwo case reports of ectodernial dysplasia in two females are presented. One case is believed to be the first reported with evidence of direct descent from mother to daughter. The other is a case of the mendelian dominant type. The submission is made that the anhydrotic type is not necessarily always a sex‐linked recessive manifestation in males ...
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SummaryTwo case reports of ectodernial dysplasia in two females are presented. One case is believed to be the first reported with evidence of direct descent from mother to daughter. The other is a case of the mendelian dominant type. The submission is made that the anhydrotic type is not necessarily always a sex‐linked recessive manifestation in males ...
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Anhidrotic ectodermal dysplasia
The Indian Journal of Pediatrics, 1968Two typical cases of anhidrotic ectodermal dysplasia occurring in heterosexual siblings of a family are reported. The role of consanguinity in the parents regarding the severity of the defect in these two siblings is stressed.
A, Bhogaonkar, S K, Khanna
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Dermatologic Clinics, 1987
In order to be considered an ectodermal dysplasia, a disorder should meet the following criteria: it must be congenital; it must be diffuse (not localized) and must involve the epidermis as well as at least one of its appendages; and it must not be progressive.
L M, Solomon, B, Cook, W, Klipfel
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In order to be considered an ectodermal dysplasia, a disorder should meet the following criteria: it must be congenital; it must be diffuse (not localized) and must involve the epidermis as well as at least one of its appendages; and it must not be progressive.
L M, Solomon, B, Cook, W, Klipfel
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ANHIDROTIC ECTODERMAL DYSPLASIA
International Journal of Dermatology, 1978ABSTRACT: Five patients with anhidrotic ectodermal dysplasia are reported from India.
B. S. N. REDDY +3 more
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Anhidrotic Ectodermal Dysplasia
Plastic and Reconstructive Surgery, 1980A diagnosis of anhidrotic ectodermal dysplasia should be considered for patients with an undeveloped breast or other deformities. Recognition of the syndrome can lead to necessary and helpful genetic counseling and will ensure that other members of the family, who may also be affected by the syndrome, are under proper care.
R A, Ersek, H, Labandter, L, King
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HEREDITARY ECTODERMAL DYSPLASIA (CONGENITAL ECTODERMAL DEFECT)
American Journal of Diseases of Children, 1929I wish to report two cases of patients who present unusual types of multiple congenital anomalies, the tissues affected in both cases having developed principally from embryonic ectoderm. Descriptions of similar patients are not lacking in the dental and medical literature, but the condition has not been specifically called to the attention of ...
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"CONGENITAL ECTODERMAL DEFECT"
Archives of Dermatology, 1924Anomalies of the epidermis and its appendages, due to faulty evolution of the epiblastic layer of the blastoderm, are numerous. In the nosology of dermatology such conditions are found among the hypertrophies, atrophies, new growths and affections of the appendages.
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