ΜΕΛΕΤΗ ΠΑΡΑΛΛΑΓΩΝ ΚΑΙ ΕΛΕΓΧΟΣ ΦΟΡΕΩΝ ΑΙΜΟΡΡΟΦΙΛΙΑΣ Β ΣΤΗΝ ΕΛΛΑΔΑ

THE HAEMOPHILIA B IS A SEX LINKED CONGENITAL HAEMORRAGIC DISORDER CAUSED BY REDUCED OR ABSENT SYNTHESIS OF FIX OF THE COAGULATION CASCADE. FIFTEEN FAMILIES CONSISTING OF 22 HAEMOPHILICS AND 61 RELATIVES WERE STUDIED. CARRIER DETECTION INASYMPTOMATIC FEMALE POSSIBLE CARRIERS WAS PERFORMED WITH CONVENTIONAL IMMUNOLOGICAL TECHNIQUES FOR EVALUATION OF THE PHENOTYPE AND WITH RESTRICTION FRAGMENT LENGTH POLYMORPHIN FOR EVALUATION OF THE DEFECT AT THE MOLECULAR LEVEL. PRENATAL DIAGNOSIS WAS PERFORMED IN 4 CASES WITH DETERMINATION OF FIX IN EMBRYONIC BLOOD. MOREOVER 37 HAEMOPHILIA 3 PATIENTS ARE CLASSIFIED ACCORDING TO SEVERITY, DEVELOPMENT OF INHIBITORS AND ANTIGENIC DETERMINANTS.

Grantor dc:publisher

National and Kapodistrian University of Athens

Year dc:date

1989

Authors dc:creator

• Γιαλεράκη-Γιακουμάκη, Αργυρή
• Gialeraki, Argiri

• Αιμορροφιλία
• ΕΛΕΓΧΟΣ ΦΟΡΕΩΝ
• ΜΟΡΙΑΚΕΣ ΠΑΡΑΛΛΑΓΕΣ
• Προγεννητικός έλεγχος
• CARRIER DETECTION
• HEAMOPHILIA
• MOLECULAR VARIANTS
• Prenatal diagnosis
• Restriction fragment length polymorphism (RFLP)
• Φυσικές Επιστήμες
• Βιολογία
• Natural Sciences
• Biological Sciences

Language dc:language

gre

Identifier

10.12681/eadd/1280

OAI identifier oai:identifier

oai:10442/1280