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Page 1
Cutaneous manifestations of gastrointestinal disease: part II.
Thrash B, Patel M, Shah KR, Boland CR, Menter A. Thrash B, et al. J Am Acad Dermatol. 2013 Feb;68(2):211.e1-33; quiz 244-6. doi: 10.1016/j.jaad.2012.10.036. J Am Acad Dermatol. 2013. PMID: 23317981 Review.
In part I of this continuing medical education article, the intricacies of this relationship were explored as they pertained to hereditary polyposis disorders, hamartomatous disorders, and paraneoplastic disease. ...Kaposi sarcoma is a neoplastic disease with lesions invol …
In part I of this continuing medical education article, the intricacies of this relationship were explored as they pertained to hereditar
Analysis of the relationship between the mutation site of the SLC39A4 gene and acrodermatitis enteropathica by reporting a rare Chinese twin: a case report and review of the literature.
Zhong W, Yang C, Zhu L, Huang YQ, Chen YF. Zhong W, et al. BMC Pediatr. 2020 Jan 27;20(1):34. doi: 10.1186/s12887-020-1942-4. BMC Pediatr. 2020. PMID: 31987033 Free PMC article. Review.
BACKGROUND: Acrodermatitis enteropathica (AE) is a rare autosomal recessive hereditary skin disease caused by mutations in the SLC39A4 gene and is characterized by periorificial dermatitis, alopecia and diarrhoea due to insufficient zinc absorption. ...
BACKGROUND: Acrodermatitis enteropathica (AE) is a rare autosomal recessive hereditary skin disease caused by mutations …
Acrodermatitis enteropathica: case report and review of the literature.
Perafán-Riveros C, França LF, Alves AC, Sanches JA Jr. Perafán-Riveros C, et al. Pediatr Dermatol. 2002 Sep-Oct;19(5):426-31. doi: 10.1046/j.1525-1470.2002.00200.x. Pediatr Dermatol. 2002. PMID: 12383101 Review.
Acrodermatitis enteropathica (AE) is a rare hereditary disorder caused by impaired absorption of zinc from the gastrointestinal tract. ...
Acrodermatitis enteropathica (AE) is a rare hereditary disorder caused by impaired absorption of zinc from the gastroin
Microelements and inherited metabolic diseases.
Marklová E. Marklová E. Acta Medica (Hradec Kralove). 2002;45(4):129-33. Acta Medica (Hradec Kralove). 2002. PMID: 12587779 Review.
In addition to the main groups of inherited metabolic diseases, including mitochondrial, peroxisomal and lysosomal defects, organic acidurias, porphyrias, defects of amino acids, saccharides and fatty acids metabolism, disorders of transport and utilisation of microelements have …
In addition to the main groups of inherited metabolic diseases, including mitochondrial, peroxisomal and lysosomal defects, organic aciduria …
[Genodermatosis in man and animal. Comparative overview].
Küster W, Happle R. Küster W, et al. Hautarzt. 1983 Nov;34(11):539-47. Hautarzt. 1983. PMID: 6358130 Review. German.
This group includes oculo-cutaneous albinism, Chediak-Higashi syndrome, aplasia cutis congenita, Ehlers-Danlos syndrome (type I), hypohidrotic ectodermal dysplasia of the Christ-Siemens-Touraine type, X-linked dominant chondrodysplasia punctata, ichthyosis congenita gravis, Menke …
This group includes oculo-cutaneous albinism, Chediak-Higashi syndrome, aplasia cutis congenita, Ehlers-Danlos syndrome (type I), hypohidrot …
[Acrodermatitis enteropathica: report of one case].
Valdés R, Mauret M, Castro Á. Valdés R, et al. Rev Med Chil. 2013 Nov;141(11):1480-3. doi: 10.4067/S0034-98872013001100017. Rev Med Chil. 2013. PMID: 24718477 Free article. Review. Spanish.
Acrodermatitis enteropathica is an uncommon disease caused by hereditary or acquired zinc deficiency. ...We report a 31-year-old indigent and drug addict female with a cutaneous-mucous syndrome characteristic of acrodermatitis enteropathica. She
Acrodermatitis enteropathica is an uncommon disease caused by hereditary or acquired zinc deficiency. ...We report a 31
[Genetics of hereditary cutaneous diseases associated with digestive tract involvement].
Desmons F, Walbaum R. Desmons F, et al. Ann Dermatol Venereol. 1979 Jan;106(1):9-12. Ann Dermatol Venereol. 1979. PMID: 384873 Review. French.
Hereditary disease with intestinal polyposis. II. Vascular dysplasias with intestinal haemorrhage. III. Connective tissue discover in hereditary diseases. IV. Acrodermatitis enteropathica with diarrhoea. ...
Hereditary disease with intestinal polyposis. II. Vascular dysplasias with intestinal haemorrhage. III. Connective tissue discover in
[Essential trace element and skin diseases].
Yamada H, Ogawa H. Yamada H, et al. Nihon Rinsho. 1996 Jan;54(1):99-105. Nihon Rinsho. 1996. PMID: 8587213 Review. Japanese.
Pigmentation of hemochromatosis and hemosiderosis are recognized by hemosiderin deposition in the dermis. Acrodermatitis enteropathica is caused by a deficiency of Zn and is classified as either a hereditary type or as an acquired type. ...
Pigmentation of hemochromatosis and hemosiderosis are recognized by hemosiderin deposition in the dermis. Acrodermatitis enteropat