By Arleen D. Auerbach Ph. D., A. Rogatko, Traute M. Schroeder-Kurth Professor Dr. med (auth.), Professor Dr. med. Traute M. Schroeder-Kurth, Arleen D. Auerbach Ph. D., Professor Dr. Günter Obe (eds.)
This monograph represents the 1st try and assemble all elements of Fanconi's anemia in a single resource. The editors are famous for his or her non-stop study within the box and feature aptly introduced jointly contributions containing the main up to date details to be had. The problems in differential analysis and therapy are coated; and the outlook for treatment through bone marrow transplantation is incorporated. This evaluate will curiosity experts in human genetics in addition to all these facing this ailment.
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Extra info for Fanconi Anemia: Clinical, Cytogenetic and Experimental Aspects
Yes 0 No D. If yes, please give reference or enclose report_ _ _ _ _ _ _ _ _ _ __ 3. Is the patient deceased? Yes 0 No 0 If deceased, date of death'--_ _ _ __ Cause of deathl-_ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ __ (Please provide autopsy report if available) 17 International Fanconi Anemia Registry: First Report 4. Does the patient have hematologic manifestations? ) 5. Medical follow-up since:_ _ _ __ a. Hospitalizations and surgery b. Acquired illnesses c. Growth and development 6.
Please indicate the ancestral groups to which the parents belong. Answer as many as apply. (P: paternal, M: maternal). P M P M P M British Isles African (Negro) Polish American Indian Scandinavian Russian German Ashkenazi Jewish Mexican Other Latin America French Sephardic Jewish Japanese Spanish Other Jewish Italian Middle Eastern Chinese North African Greek Other Asian Other (please specify),_ _ _ _ _ _ _ _ _ _ _ _ __ Turkish e. Siblings: Number (full)_ _ (half)-List below, in order of pregnancy, all full and half siblings of the patient.
There is no correlation between the severity of the anomalies and the course of the disease. FA patients with several anomalies and especially those with radial ray defects were diagnosed earlier than those patients without anomalies. The sex ratio among pro bands shows a (nonsignificant) male preponderance, in accordance with previous reports (Alter and Potter 1983). This suggests a better ascertainment of affected male probands, since the sex ratio among affected sibs is close to 1 : 1. A better ascertainment of male probands cannot be explained since there are no FA-specific genital abnormalities: cryptorchidism is the only sexlinked anomaly which is easily identified and frequently observed on physical examination but no indication for FA.
Fanconi Anemia: Clinical, Cytogenetic and Experimental Aspects by Arleen D. Auerbach Ph. D., A. Rogatko, Traute M. Schroeder-Kurth Professor Dr. med (auth.), Professor Dr. med. Traute M. Schroeder-Kurth, Arleen D. Auerbach Ph. D., Professor Dr. Günter Obe (eds.)