Literature DB >> 9694334

Kabuki make-up syndrome and report of a case with hydrocephalus.

H Kasuya1, T Shimizu, S Nakamura, K Takakura.   

Abstract

We report a 22-year-old man with hydrocephalus caused by aqueductal stenosis. The patient was diagnosed with Kabuki make-up syndrome based on associated findings such as a peculiar facies, postnatal growth deficiency, brachydactyly of the fifth fingers, undescended testes, and malrotation of the colon. Kabuki make-up syndrome, recognized in Japan in 1981, is characterized by five cardinal manifestations: a peculiar facies, skeletal anomalies, dermatoglyphic anomalies, slight to moderate mental retardation, and postnatal dwarfism. Neurological anomalies have been reported to include neonatal hypotonia, feeding problems, seizures, West syndrome, microcephaly, brain atrophy, GH deficiency, precocious puberty, delayed sexual development, and diabetes insipidus. Aqueductal stenosis may be caused by part of the series of midline anomalies. Physicians should pay attention to associated anomalous characteristics suggesting a malformation syndrome when they encounter nontumoral aqueductal stenosis in adolescents or adults.

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Year:  1998        PMID: 9694334     DOI: 10.1007/s003810050218

Source DB:  PubMed          Journal:  Childs Nerv Syst        ISSN: 0256-7040            Impact factor:   1.475


  4 in total

1.  [Niikawa-Kuroki (Kabuki) syndrome and hearing impairment].

Authors:  K Lüerssen; M Ptok
Journal:  HNO       Date:  2004-05       Impact factor: 1.284

2.  Facial Dysmorphisms, Macrodontia, Focal Epilepsy, and Thinning of the Corpus Callosum: A Rare Mild Form of Kabuki Syndrome.

Authors:  Valentina Bruni; Cristina Scozzafava; Maria Gnazzo; Francesca Parisi; Simona Sestito; Licia Pensabene; Antonio Novelli; Daniela Concolino
Journal:  J Pediatr Genet       Date:  2020-02-17

3.  Carotid artery occlusion in Kabuki syndrome: Case report and literature review.

Authors:  Luana A M Gatto; Luis Henrique A Sousa; Gelson Luis Koppe; Zeferino Demartini
Journal:  Surg Neurol Int       Date:  2017-05-26

4.  Novel KDM6A splice-site mutation in kabuki syndrome with congenital hydrocephalus: a case report.

Authors:  Zhimei Guo; Fang Liu; Hai Jun Li
Journal:  BMC Med Genet       Date:  2018-12-03       Impact factor: 2.103

  4 in total

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