Yq<sub>TER</sub> deletion causes arrest of spermatogenesis in early puberty

dc.contributor.authorCastro, A
dc.contributor.authorZambrano, N
dc.contributor.authorKaune, H
dc.contributor.authorMadariaga, M
dc.contributor.authorLópez, P
dc.contributor.authorMericq, V
dc.date.accessioned2025-01-21T01:07:24Z
dc.date.available2025-01-21T01:07:24Z
dc.date.issued2004
dc.description.abstractWe report a 12-7/12 year-old male with obesity, eunuchoid proportions, genetic stigmata of Turner's syndrome and mild developmental delay. We investigated whether cytogenetic alterations could be responsible for his phenotype. Conventional karyotype in 70 peripheral blood cells was 45,X(15%)/46,XYqh-(85%). Dual FISH on 1,000 nuclei revealed 8% of X0 cells (DXZ1 X-centromeric probe) and 92% of XY cells (DYZ3 Y-centromeric probe). We studied Y chromosome microdeletions by PCR. The patient showed a terminal Yq deletion from the 51 interval including the AZFb and AZFc regions. FSH, LH and testosterone (468 ng/dl) were within the normal range for his age. At Tanner IV pubertal development the spermiogram showed azoospermia and the testicular aspirate spermatic arrest. The present report suggests that Y chromosome deletions including AZFb and AZFc regions may cause spermatogenic arrest in early puberty.
dc.fuente.origenWOS
dc.identifier.eissn2191-0251
dc.identifier.issn0334-018X
dc.identifier.urihttps://repositorio.uc.cl/handle/11534/96324
dc.identifier.wosidWOS:000226087000013
dc.issue.numero12
dc.language.isoen
dc.pagina.final1678
dc.pagina.inicio1675
dc.revistaJournal of pediatric endocrinology & metabolism
dc.rightsacceso restringido
dc.subjectY chromosome deletion
dc.subjectadolescence
dc.subjectspermiogenic maturation
dc.subjectarrest of spermatogenesis
dc.subject.ods03 Good Health and Well-being
dc.subject.odspa03 Salud y bienestar
dc.titleYq<sub>TER</sub> deletion causes arrest of spermatogenesis in early puberty
dc.typeartículo
dc.volumen17
sipa.indexWOS
sipa.trazabilidadWOS;2025-01-12
Files