Publication:
Two patients with Kabuki syndrome presenting with endocrine problems

dc.contributor.authorsBereket A., Turan S., Alper G., Comu S., Alpay H., Akalin F.
dc.date.accessioned2022-03-15T01:54:11Z
dc.date.accessioned2026-01-10T20:34:52Z
dc.date.available2022-03-15T01:54:11Z
dc.date.issued2001
dc.description.abstractA 4 year-old boy with mental retardation and seizures presented to the pediatric endocrinology clinic because of a history of hypoglycemia; a 16 month-old girl with developmental delay presented with bilateral breast tissue enlargement; in both, a diagnosis of Kabuki syndrome was made because of typical facial features, neurodevelopmental delay and other stigmata consistent with Kabuki syndrome. Kabuki syndrome is a mental retardation-malformation syndrome affecting multiple organ systems with a broad spectrum of abnormalities. The facial features of the syndrome are specific and independent of ethnic origin. In addition to presenting with endocrine problems, the patients reported here exhibit some novel findings such as congenital alopecia areata and hyperpigmented skin lesion. The diagnosis of Kabuki syndrome should be considered in patients with hypoglycemia or premature thelarche when associated with developmental delay and a peculiar facies.
dc.identifier.doi10.1515/JPEM.2001.14.2.215
dc.identifier.issn0334018X
dc.identifier.pubmed11305802
dc.identifier.urihttps://hdl.handle.net/11424/246483
dc.language.isoeng
dc.publisherFreund Publishing House Ltd
dc.relation.ispartofJournal of Pediatric Endocrinology and Metabolism
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectHypoglycemia
dc.subjectKabuki syndrome
dc.subjectMalformation
dc.subjectMental retardation
dc.subjectPremature thelarche
dc.titleTwo patients with Kabuki syndrome presenting with endocrine problems
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPage220
oaire.citation.issue2
oaire.citation.startPage215
oaire.citation.titleJournal of Pediatric Endocrinology and Metabolism
oaire.citation.volume14

Files