Married couple both with myeloproliferative disorder and chromosome 3 abnormality
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چکیده
منابع مشابه
Northern Wisconsin married couple infected with blastomycosis.
Blastomycosis is an uncommon, chronic, granulomatous disease caused by the dimorphic fungus Blastomycosis dermatitidis. The great majority of infections start with primary pulmonary involvement through inhalation of spores. Hematogenous dissemination to other sites occurs in 25% to 30% of cases. The most common secondary site is the skin, followed in order by bone, genitourinary system, and cen...
متن کاملPolymyalgia rheumatica in a married couple
The case of a married couple developing polymyalgia rheumatica (PMR) consecutively is presented. The 55-year-old wife complained in June 2010 about pain in her neck. Case history, physical examination, and erythrocyte sedimentation rate (ESR) of 80 mm/hour led to the diagnosis of PMR. In May 2011, her 66-year old husband complained about pain in his neck, shoulders, buttocks, and thighs. Consid...
متن کاملThe Effectiveness of Emotionally-Focused Couple Therapy on Happiness and Quality of Married Life of Both Working Couples
The present study aimed to Determine the effectiveness of emotionally-focused couple therapy on happiness and quality of married life of dual-career couples. The method of study was quasi-experimental with a pre-test-post-test design with a control group. The statistical population included all working couples referred to Alborz Counseling Center in Karaj from the second half of October to the ...
متن کاملPsychotic disorder and focal epilepsy in a left-handed patient with chromosome XYY abnormality.
OBJECTIVE To discuss the relationship between XYY chromosome abnormality, psychiatric disorders and epilepsy. METHOD Single case report. RESULTS A 34-year-old man with 47, XYY karyotype and normal intelligence was followed-up at a neuropsychiatric clinic for over 30 years. He was first seen at age 3 years with a history of delayed motor and language development and an immunodeficiency syndr...
متن کاملAplasia cutis congenita with chromosome 12q abnormality.
A 32 week, small for dates baby with aplasia cutis congenita had an unbalanced translocation, being monosomic for distal 12q and trisomic for distal 1q. As far as is known, the association between extensive skin defects and a chromosomal abnormality has not been reported before. Keratin genes have been located in a different area of 12q, but this case may indicate other candidate areas to explo...
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ژورنال
عنوان ژورنال: American Journal of Hematology
سال: 1998
ISSN: 0361-8609,1096-8652
DOI: 10.1002/(sici)1096-8652(199805)58:1<91::aid-ajh19>3.3.co;2-o