8p11.2 deletion syndrome

8p11.2 deletion syndrome is a contiguous gene syndrome characterized by the association of congenital spherocytosis, dysmorphic features, growth delay and hypogonadotropic hypogonadism.

Azoospermia

Absence of any measurable level of sperm in his semen.


合計: 0

                       


（表示件数）
PMID (PMCID)