نتایج جستجو برای: acrodermatitis enthropathica

تعداد نتایج: 473  

Journal: :مجله دانشگاه علوم پزشکی شهید صدوقی یزد 0
راضیه فلاح r fallah

biotin is a water-soluble vitamin and co-factor for activation of carboxylases apoenzymes. biotinidase enzyme is essential for release of biotin from apoenzymes. absence of biotinidase is an autosomal recessive trait with a prevalence of 1 in 60000. clinical manifestations of biotinidase deficiency include dermatitis, alopecia, seizures, hypotonia, developmental delay, hearing loss, visual impa...

Biotin is a water-soluble vitamin and co-factor for activation of carboxylases apoenzymes. Biotinidase enzyme is essential for release of biotin from apoenzymes. Absence of biotinidase is an autosomal recessive trait with a prevalence of 1 in 60000. Clinical manifestations of biotinidase deficiency include dermatitis, alopecia, seizures, hypotonia, developmental delay, hearing loss, visual impa...

Journal: :Gut 1989
D Mack B Koletzko S Cunnane E Cutz A Griffiths

We report a patient with acrodermatitis enteropathica and a normal serum zinc level in whom the diagnosis was confirmed by plasma phospholipid fatty acid and a small bowel biopsy response to oral zinc therapy. Acrodermatitis enteropathica is a rare autosomal recessive condition of zinc deficiency characterised by chronic diarrhoea associated with failure to thrive, periorificial dermatitis and ...

2002
Byung Chul Kim Kwang Ro Joo Hyo Sup Lee Yoong Ki Jeong Ho Seok Suh Do Ha Kim Neung Hwa Park Jae Hoo Park

Liver infarction and acrodermatitis enteropathica are rare complications of chronic pancreatitis. This report shows the case of a 56-year-old man who developed liver infarction due to portal vein thrombosis from chronic pancreatitis and acrodermatitis enteropathica during the course of his treatment. The rare combination of these complications in a patient with chronic pancreatitis has never pr...

Journal: :Infection and immunity 2007
Robert R Müllegger Terry K Means Junghee J Shin Marshall Lee Kathryn L Jones Lisa J Glickstein Andrew D Luster Allen C Steere

The three skin disorders of Lyme borreliosis in Europe include erythema migrans, an acute, self-limited lesion; borrelial lymphocytoma, a subacute lesion; and acrodermatitis chronica atrophicans, a chronic lesion. Using quantitative reverse transcription-PCR, we determined mRNA expression of selected chemokines, cytokines, and leukocyte markers in skin samples from 100 patients with erythema mi...

2010
Zerrin Orbak Vildan Ertekin Ayse Selimoglu Nebahat Yilmaz Huseyin Tan Murat Konak

This report describes an 11-month old girl with Hartnup disease presenting with kwashiorkor and acrodermatitis enteropathica-like skin lesions but free of other clinical findings. This case with kwashiorkor had acrodermatitis enteropathica-like desquamative skin eruption. Since zinc level was in the normal range, investigation for a metabolic disorder was considered, and Hartnup disease was dia...

Journal: :Molecular pathology : MP 1997
M M Picken R N Picken D Han Y Cheng E Ruzic-Sabljic J Cimperman V Maraspin S Lotric-Furlan F Strle

AIM To compare polymerase chain reaction (PCR) amplification of borrelial DNA and culture isolation of spirochaetes for the diagnosis of Lyme borreliosis by direct detection of Borrelia burgdorferi sensu lato in patients with erythema migrans and acrodermatitis chronica atrophicans lesions. METHODS Skin biopsy specimens from erythema migrans and acrodermatitis chronica atrophicans lesions wer...

Journal: :Boletín Médico del Hospital Infantil de México 2017

Journal: :Proceedings of the Royal Society of Medicine 1929

Journal: :JAAD case reports 2016
Allison P Weinkle Nishit Patel Rebecca Kissel Lucia Seminario-Vidal

AE: acrodermatitis enteropathica CD: celiac disease GFD: gluten-free diet INTRODUCTION Cutaneous manifestations can occur in association with various gastrointestinal diseases. When dermatitides present in the setting of unintentional weight loss before a gastrointestinal disease is diagnosed, early recognition can aid in the diagnosis of nutritional deficiency secondary to malabsorption. A cas...

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