منابع مشابه
Chromosome studies in familial leukaemia.
The finding of an inherited chromosome abnormality (Chl) in several members of a family, including two who had developed chronic lymphocytic leukaemia (Gunz, Fitzgerald, and Adams, i962), led to the suggestion that this abnormality predisposed its carriers to the development of the disease, and that inherited cytogenetic abnormalities of this type might determine some instances of familial leuk...
متن کاملFamilial neonatal leukaemia.
Recently there has been considerable discussion in the literature about possible genetic factors in the aetiology of leukaemia. These have been summarized and discussed by Steinberg (1960). All authorities agree that it is rare to find more than one case of leukaemia among the children of a family, although cases occurring in cousins, uncle and nephew, etc., are less unusual. An additional feat...
متن کاملFamilial occurrence of chronic lymphocytic leukaemia in Norway.
BACKGROUND The only known risk factor for chronic lymphocytic leukaemia (CLL) is occurrence of the disease in close relatives. The aim of this study was to determine the frequency of familial chronic lymphocytic leukaemia. MATERIAL AND METHOD All patients with chronic lymphocytic leukaemia notified to the Cancer Registry in the period 1.10.2007-31.12.2009 were asked to report occurrences of m...
متن کاملPatients in Focus: What’s Relevant for Chronic Myeloid Leukaemia and Philadelphia Chromosome-positive Acute Lymphoblastic Leukaemia?
EMJ EUROPEAN MEDICAL JOURNAL HEMATOLOGY • August 2017 • Creative Commons Attribution-Non Commercial 4.0 EMJ EUROPEAN MEDICAL JOURNAL 52 53 PATIENTS IN FOCUS: WHAT’S RELEVANT FOR CHRONIC MYELOID LEUKAEMIA AND PHILADELPHIA CHROMOSOME-POSITIVE ACUTE LYMPHOBLASTIC LEUKAEMIA? This satellite symposium took place on 22nd June 2017 as part of the 22nd European Hematology Association (EHA) Congress in M...
متن کاملPractice of Consanguinity and Unusual Cases of Inherited Familial Chromosome Abnormalities: A Case Report
We present 2 cases of likely rare event. In case 1, 3rd degree consanguineous marriage revealed inv(6) with same break points in parents who were found to be phenotypically normal. The same inv(6) being inherited in progeny but presented with low AMH (anti Mullerian hormone) and high level of FSH (follicular stimulating hormone) leading to polycystic ovarian syndrome/premature ovarian failure. ...
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ژورنال
عنوان ژورنال: Journal of Medical Genetics
سال: 1966
ISSN: 1468-6244
DOI: 10.1136/jmg.3.2.96