Literature DB >> 15690369

Neonatal phenotype in Kabuki syndrome.

Keith K Vaux1, Louanne Hudgins, Lynne M Bird, Elizabeth Roeder, Cynthia J R Curry, Marilyn Jones, Kenneth L Jones.   

Abstract

The Kabuki syndrome is a well-established pattern of human malformation with readily recognizable features, however the diagnosis is rarely made in the newborn period. The purpose of this study was to determine if there exists a neonatal phenotype for this disorder. We ascertained 16 infants evaluated in the first 28 days of life by a dysmorphologist who subsequently received the diagnosis of Kabuki syndrome. The average age of initial evaluation was 8 days and the average age of diagnosis was 2 years 6 months. Based on these findings, it is suggested that the distinctive clinical phenotype seen in older patients is also evident in the newborn period.

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Year:  2005        PMID: 15690369     DOI: 10.1002/ajmg.a.30336

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  8 in total

1.  Infrequent Manifestations of Kabuki Syndrome in a Patient with Novel MLL2 Mutation.

Authors:  Y A Zarate; H Zhan; J R Jones
Journal:  Mol Syndromol       Date:  2012-08-30

2.  Surgical treatment of hip dislocation in Kabuki syndrome: use of incomplete periacetabular osteotomy for posterior acetabular wall deficiency.

Authors:  Akifusa Wada; Tomoyuki Nakamura; Toru Yamaguchi; Haruhisa Yanagida; Kazuyuki Takamura; Yutaka Oketani; Hideaki Kubota; Toshio Fujii
Journal:  J Child Orthop       Date:  2012-07-24       Impact factor: 1.548

3.  Hypoplastic left heart syndrome in patients with Kabuki syndrome.

Authors:  Grace C Kung; Philip M Chang; Mark S Sklansky; Linda M Randolph
Journal:  Pediatr Cardiol       Date:  2009-12-05       Impact factor: 1.655

4.  Neonatal hyperinsulinemic hypoglycemia: case report of kabuki syndrome due to a novel KMT2D splicing-site mutation.

Authors:  Ettore Piro; Ingrid Anne Mandy Schierz; Vincenzo Antona; Maria Pia Pappalardo; Mario Giuffrè; Gregorio Serra; Giovanni Corsello
Journal:  Ital J Pediatr       Date:  2020-09-18       Impact factor: 2.638

5.  Clinical exome sequencing for fetuses with ultrasound abnormalities and a suspected Mendelian disorder.

Authors:  Elizabeth A Normand; Alicia Braxton; Salma Nassef; Patricia A Ward; Francesco Vetrini; Weimin He; Vipulkumar Patel; Chunjing Qu; Lauren E Westerfield; Samantha Stover; Avinash V Dharmadhikari; Donna M Muzny; Richard A Gibbs; Hongzheng Dai; Linyan Meng; Xia Wang; Rui Xiao; Pengfei Liu; Weimin Bi; Fan Xia; Magdalena Walkiewicz; Ignatia B Van den Veyver; Christine M Eng; Yaping Yang
Journal:  Genome Med       Date:  2018-09-28       Impact factor: 11.117

6.  Case Report: An Infant With Kabuki Syndrome, Alobar Holoprosencephaly and Truncus Arteriosus: A Case for Whole Exome Sequencing in Neonates With Congenital Anomalies.

Authors:  Rishika P Sakaria; Parul G Zaveri; Shannon Holtrop; Jie Zhang; Chester W Brown; Eniko K Pivnick
Journal:  Front Genet       Date:  2021-11-25       Impact factor: 4.599

7.  Genome-wide DNA methylation profiling confirms a case of low-level mosaic Kabuki syndrome 1.

Authors:  Carolina Montano; Jacquelyn F Britton; Jacqueline R Harris; Jennifer Kerkhof; Benjamin T Barnes; Jennifer A Lee; Bekim Sadikovic; Nara Sobreira; Jill A Fahrner
Journal:  Am J Med Genet A       Date:  2022-04-06       Impact factor: 2.578

8.  Diagnosis and Management of Hip Dislocation in Patients with Kabuki Syndrome.

Authors:  Chaemoon Lim; Sung-Taek Jung; Chang Ho Shin; Moon Seok Park; Won Joon Yoo; Chin Youb Chung; In Ho Choi; Jung Min Ko; Tae-Joon Cho
Journal:  Clin Orthop Surg       Date:  2019-11-12
  8 in total

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