Results 231 to 240 of about 18,314 (251)
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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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Arthrogryposis and Ectodermal Dysplasia
Human Heredity, 1982Arthrogryposis, an unusual type of ectodermal dysplasia, growth retardation of prenatal onset, and diabetes mellitus were all present in the proposita and are unlikely to have arisen all independently. The combination of at least some of these abnormalities may represent a distinct syndrome.
S. Pantelakis +2 more
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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, B. Letot, D. Van Neste
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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, B. Letot, D. Van Neste
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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.
S. K. Khanna, Anant Bhogaonkar
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Archives of Dermatology, 1982
To the Editor.— We read the article by Solomon and Keuer in the November 1980Archives(116:1295-1299) and the article by Hazen et al in the December 1980Archives(116:1385-1387) on ectodermal dysplasia (ED) and would like to offer some comments to elucidate some topics.
Marta Pinheiro, Newton Freire‐Maia
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To the Editor.— We read the article by Solomon and Keuer in the November 1980Archives(116:1295-1299) and the article by Hazen et al in the December 1980Archives(116:1385-1387) on ectodermal dysplasia (ED) and would like to offer some comments to elucidate some topics.
Marta Pinheiro, Newton Freire‐Maia
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Keratoprosthesis in Ectodermal Dysplasia
Cornea, 2016To describe the complex surgical management and novel medical approach for a keratoprosthesis (KPro Boston type I) in a monocular, 73-year-old patient with ectodermal dysplasia and chronic, noninfectious corneal necrosis.Best-corrected visual acuity (BCVA) was measured with Snellen letters.
Mithra O. Gonzalez +2 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.
Robert A. Ersek +2 more
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Children With Ectodermal Dysplasias
Journal of School Health, 1998I wish I had information about Michael̂s condition, ectodermal dysplasia, to give his teachers at the beginning of every school year. They don't seem to understand his condition and what can be done to prevent problems from developing in the classroom. He's missed school days unnecessarily.
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Otodental dysplasia: a “new” ectodermal dysplasia
Clinical Genetics, 1975Otodental dysplasia is an ectodermal dysplasia characterized by abnormal crown morphology of the teeth and sensorineural hearing loss. It was documented in six generations of a kindred of Italian extraction. Thirty‐three of the 119 examined family members were affected. Twenty‐six persons had characteristic dental anomalies combined with a hearing loss.
Roger A. Cook +2 more
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