[Disorders of O2 transport and their correction in heart surgery patients].

Basic factors of O2 transport disturbances and mechanisms of their compensation have been studied in 1200 patients after cardiac surgery. It has been shown that O2 transport decrease is induced by damages in oxygenating blood function, decreased cardiac performance and hemoglobin blood level, oxyhemoglobin dissociation curve deviation and changes in Hb affinity to O2 with regard to 2,3-DPG content. The causes of arterial O2 transport damage affect the treatment procedures, including oxygen therapy, controlled lung ventilation, erythrocyte mass transfusion, inotropic drug administration, hypothermia.

Malformations of the umbilical cord.

In 184 autopsies of death newborns, stillborn infants and aborted fetuses (mostly with congenital malformations), 57 (30.98%) umbilical cord anomalies were discovered (38 M and 19 F): 19 cases with knots (10.32%), 17 with arterial agenesis (9.

Morphological and cytogenetic studies on conjoined twins.

Two cases of monoamniotic conjoined male twins, born at term after normal pregnancies, are reported. The first case, a bicephalus, shows hypoplastic and malformed left-side organs, absence of the left umbilical artery, and two communicating hearts, the left one with three cameras. The second case, a pygothoracopagus, consists in a twin "parasite", with no head but with two upper and two lower limbs, slightly less developed than those of the formed twin.

[Hereditary nephritis with bearing loss of the receiver type (Alport's syndrome) with a description of 2 cases].

A familial predisposed diffuse nephropathy is described in three adult patients--brothers, combined with hearing abatement--receiver type--in two of them. Typical gout was also found in them, that is difficult to associate with the azotemia. It was admitted that it concerns the Alport syndrome in adults, developing with certain peculiarities, advanced patient age, disturbances of purine metabolism, moderately selective proteinuria of glomercultubular type and chromosome aberration--thresomia of F chromosome.