Vertaling van "holoprosencephaly with caudal dysgenesis syndrome " (Engels → Frans) :

Holoprosencephaly with caudal dysgenesis syndrome
syndrome d'holoprosencéphalie-dysgénésie caudale

Klinefelter's syndrome | Klinefelter-Reifenstein-Albright syndrome | chromatin-positive microorchidism | gynecomastia-aspermatogenesis syndrome | medullary gonadal dysgenesis | primary micro-orchidism | pseudohermaphroditism with gonadal dysgenesis | puberal seminiferous tubule failure | seminiferous tubule dysgenesis | sclerosing tubular degeneration | testicular disgenesis | XXY syndrome
syndrome de Klinefelter | Syndrome de Klinefelter-Reifenstein-Albright

Klinefelter's syndrome [ Klinefelter-Reifenstein-Albright syndrome | chromatin-positive microorchidism | gynecomastia-aspermatogenesis syndrome | medullary gonadal dysgenesis | primary micro-orchidism | pseudohermaphroditism with gonadal dysgenesis | puberal seminiferous tubule failure | semin ]
syndrome de Klinefelter [ syndrome de Klinefelter-Reinfenstein-Albright ]

An extremely rare disorder of sex development, reported in only two siblings to date. The syndrome has clinical features of 46,XY complete gonadal dysgenesis in association with severe dwarfism with generalised chondrodysplasia (bell-shaped thorax, m
syndrome de chondrodysplasie-anomalie du développement sexuel

Syndrome with characteristics of caudal appendage, short terminal phalanges, deafness, cryptorchidism, intellectual deficit, short stature and dysmorphism. It has been described in monozygotic twin boys.
syndrome d'appendice caudal-surdité