A Patient with Tyrosine Kinase 2 Deficiency without Hyper-IgE Syndrome
نویسندگان
چکیده
منابع مشابه
Cutis verticis gyrata in a patient with hyper-IgE syndrome.
© 2009 The Authors. doi: 10.2340/00015555-0652 Journal Compilation © 2009 Acta Dermato-Venereologica. ISSN 0001-5555 Sir, Cutis verticis gyrata (CVG) is a rare morphological condition of the scalp characterized by ridges and furrows resembling the surface of the brain. We report here a case of CVG in a patient with hyper-IgE syndrome, which is a multisystem disorder known to affect the dentitio...
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hyper - immunoglobulin e syndrome is a rare primary immunodeficiency disease characterized by recurrent abscess formation, respiratory tract infections and very high titers of serum ige associated with peculiar face and skeletal features. we report a seven-year old girl presenting with persistent productive cough and history of chronic eczematoid facial lesions since infancy and two episod...
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Hyper IgE syndrome (Job’s syndrome) is a primary immunodeficiency disease with recurrent infections especially staphylococcal, coarse face, skeletal abnormality and significant increase in serum IgE level (IgE >2000IU/ml). We present a 16 years old boy admitted with chronic cough, dyspnea, eczema and pneumatocele. He had a history of chronic dermal infection since 1 month after birth. The dia...
متن کاملPsoriasis in hyper IgE syndrome – a case report
Background: Hyper IgE syndrome (HIES) is a rare primary immune deficiency, described as Job`s syndrome characterized by increased serum levels of IgE, eczema, recurrent cutaneous and pulmonary infections. In this paper, we presented a case of Hyper IgE syndrome.Case Presentation: A 16-year-old Iranian boy presented with a one year history of skin lesions in knees and elbows was diagnosed of pso...
متن کاملHuman TYK2 deficiency: Mycobacterial and viral infections without hyper-IgE syndrome
Autosomal recessive, complete TYK2 deficiency was previously described in a patient (P1) with intracellular bacterial and viral infections and features of hyper-IgE syndrome (HIES), including atopic dermatitis, high serum IgE levels, and staphylococcal abscesses. We identified seven other TYK2-deficient patients from five families and four different ethnic groups. These patients were homozygous...
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ژورنال
عنوان ژورنال: The Journal of Pediatrics
سال: 2012
ISSN: 0022-3476
DOI: 10.1016/j.jpeds.2012.01.056