Indexed keywords
ANHIDROTIC ECTODERMAL DYSPLASIA;
ARTICLE;
AUTOSOMAL RECESSIVE INHERITANCE;
CASE REPORT;
CLINICAL FEATURE;
FOOT SOLE;
HAND PALM;
HUMAN;
HYPERPYREXIA;
HYPODONTIA;
HYPOTRICHOSIS;
KERATOSIS PALMOPLANTARIS;
MALE;
SCHOOL CHILD;
SKIN BIOPSY;
SWEAT GLAND DISEASE;
THICKNESS;
TOOTH MALFORMATION;
X CHROMOSOME LINKED DISORDER;
CHILD;
ECTODERMAL DYSPLASIA 1, ANHIDROTIC;
GENES, X-LINKED;
HUMANS;
KERATODERMA, PALMOPLANTAR;
MALE;
PEDIGREE;
SKIN;
SYNDROME;
1
0003064569
Two cases in which the skin, hair and teeth were very imperfectly developed
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Thurnam, J.1
2
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The major forms of hereditary ectodermal dysplasia
Clouston HR. The major forms of hereditary ectodermal dysplasia. Can Med Assoc J 1939; 40: 1-7.
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Clouston, H.R.1
3
0028989078
Verruciform palmoplantar keratoderma as a characteristic marker of hidrotic ectodermal dysplasia of the clouston type
Koch P, Foss P, Baum HP, et al. Verruciform palmoplantar keratoderma as a characteristic marker of hidrotic ectodermal dysplasia of the clouston type. Hautarzt 1995; 46: 272-275.
(1995)
Hautarzt , vol.46
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Koch, P.1
Foss, P.2
Baum, H.P.3
4
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A toothless type of man
Thadani KI. A toothless type of man. J Hered 1921; 12: 87-88.
(1921)
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Thadani, K.I.1
5
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Gene localization of X-linked hypohidrotic ectodermal dyspalsia (C-S-T)
MacDermont KD, Winter RM, Malcom S. Gene localization of X-linked hypohidrotic ectodermal dyspalsia (C-S-T). Hum Genet 1986; 74: 172-173.
(1986)
Hum Genet , vol.74
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MacDermont, K.D.1
Winter, R.M.2
Malcom, S.3
6
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X-linked anhidrotic ectodermal dysplasia is caused by mutation in a novel transmembrane protein
Kere J, Srivastava AK, Montonen O, et al. X-linked anhidrotic ectodermal dysplasia is caused by mutation in a novel transmembrane protein. Nature Genet 1996; 13: 409-416.
(1996)
Nature Genet , vol.13
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Kere, J.1
Srivastava, A.K.2
Montonen, O.3
7
0029977754
Reduced epidermal growth factor receptor expression in hypohidrotic ectodermal dysplasia and tabby mice
Vargas GA, Fantino E, George-Nascimento C, et al. Reduced epidermal growth factor receptor expression in hypohidrotic ectodermal dysplasia and tabby mice. J Clin Inv 1996; 97: 2426-2432.
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J Clin Inv , vol.97
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Vargas, G.A.1
Fantino, E.2
George-Nascimento, C.3
8
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Christ-Siemens-Touraine syndrome - A clinical and genetic study analysis of large Brazilian kindred
Pinheiro M, Freirie-Maia N. Christ-Siemens-Touraine syndrome - a clinical and genetic study analysis of large Brazilian kindred. Am J Med Genet 1979; 4: 113-122.
(1979)
Am J Med Genet , vol.4
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Pinheiro, M.1
Freirie-Maia, N.2
9
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Hereditary anhidrotic ectodermal dysplasia. A clinical and pathologic study
Upshaw BY, Mantogmery H. Hereditary anhidrotic ectodermal dysplasia. A clinical and pathologic study. Arch Dermatol Syphilol 1949; 60: 1170-1183.
(1949)
Arch Dermatol Syphilol , vol.60
, pp. 1170-1183
Upshaw, B.Y.1
Mantogmery, H.2
10
0014833344
Clinical spectrum of anhidrotic ectodermal dysplasia
Reed WB, Lopez DA, Landing BH. Clinical spectrum of anhidrotic ectodermal dysplasia. Arch Dermatol 1970; 102: 134-143.
(1970)
Arch Dermatol , vol.102
, pp. 134-143
Reed, W.B.1
Lopez, D.A.2
Landing, B.H.3
11
2642650915
Hereditary ectodermal dysplasia associated with primary hypogonadism
Mohler DN. Hereditary ectodermal dysplasia associated with primary hypogonadism. Am J Med 1959; 27: 682-688.
(1959)
Am J Med , vol.27
, pp. 682-688
Mohler, D.N.1
12
0023230573
Hypohidrotic ectodermal dysplasia
Clarke A. Hypohidrotic ectodermal dysplasia. J Med Genet 1987; 24: 659-663.
(1987)
J Med Genet , vol.24
, pp. 659-663
Clarke, A.1
13
0025158443
Unusual cutaneous manifestations of anhidrotic ectodermal dysplasia - A case report
Shah KC, Umrigar DD. Unusual cutaneous manifestations of anhidrotic ectodermal dysplasia - a case report. J Dermatol 1990; 17: 380-384.
(1990)
J Dermatol , vol.17
, pp. 380-384
Shah, K.C.1
Umrigar, D.D.2
