Results 41 to 50 of about 2,564 (144)
Acquired zinc deficiency in an adult female
Indian Journal of Dermatology, 2012 Acrodermatitis enteropathica is an autosomal recessive inherited disorder of zinc absorption. Acquired cases are reported occasionally in patients with eating disorders or Crohn′s disease.
Mohanan Saritha +4 more
doaj +1 more source
Microelements and Inherited Metabolic Diseases
Acta Medica, 2002 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 ...
Eliška Marklová
doaj +1 more source
Acrodermatitis enteropathica-like changes in a patient with parenteral nutrition
, 1999 Löffler H, Effendy I. Acrodermatitis- enteropathica-ähnliche Hautveränderungen durch parenterale Ernährung. Hautarzt. 1999;50(7):499-502.A patient on long term parenteral nutrition developed acrodermatitis enteropathica-like skin changes.
Effendy, Isaak ; https://orcid.org/ +1 more
core +1 more source
Acrodermatitis dysmetabolica as a sign of methylmalonic aciduria decompensation
Clinical Case Reports, 2018 Key Clinical Message Methylmalonic aciduria children must follow an adequate diet with low protein intake and should be regularly monitored to prevent complications.
Joana Rosa +5 more
doaj +1 more source
, 2009 Background: Acrodermatitis acidemica is a recently proposed term for the rash that is similar to acrodermatitis enteropathica, which is encountered in organic acidemias.
Tabanhoglu, Duru +5 more
core +1 more source
A mouse model of acrodermatitis enteropathica: loss of intestine zinc transporter ZIP4 (Slc39a4) disrupts the stem cell niche and intestine integrity. [PDF]
PLoS Genetics, 2012 Mutations in the human Zip4 gene cause acrodermatitis enteropathica, a rare, pseudo-dominant, lethal genetic disorder. We created a tamoxifen-inducible, enterocyte-specific knockout of this gene in mice which mimics this human disorder. We found that the
Jim Geiser +3 more
doaj +1 more source
Acrodermatitis enteropathica secondary to Crohn's disease.
, 1996 A patient suffering from Crohn's disease (CD) presented with alopecia, eczematoid and psoriasiform lesions located on the extremities, around the orifices and at pressure points, suggesting acrodermatitis enteropathica.
Frenk E, Krasovec M
core +1 more source
Clinical Case Reports, Volume 14, Issue 7, July 2026.ABSTRACT Multiple carboxylase deficiency (MCD) is a rare, treatable inborn error of biotin metabolism that may present in children in the first year of life with life‐threatening metabolic crises. We report a 4‐month‐old child presenting with persistent seizures, eczematous rash near the orifices, unjustified loss of hair with baldness, and severe ...
Touqeer Rehman +8 more
wiley +1 more source
Acrodermatitis enteropathica with Pseudomonas aeruginosa sepsis
, 1999 Acrodermatitis enteropathica is characterized by eczematous and scaly plaques on the face, scalp, acral, and anogenital regions, In addition to typical lesions, unusual prominent vesiculobullous lesions are also described.
Ozkan, H +5 more
core +1 more source
Central European Journal of Immunology, 2022 We present a case of a white adult female patient who suffered from chronic mucocutaneous candidiasis (CMC) since infancy. Her parents were not consanguineous, and neither of them nor any other family member, including an older sister, suffered from ...
Stanisława Bazan-Socha +5 more
doaj +1 more source