Literature DB >> 26829900

ALDH18A1-related cutis laxa syndrome with cyclic vomiting.

Fumihito Nozaki1, Takashi Kusunoki2, Nobuhiko Okamoto3, Yuto Yamamoto3, Fuyuki Miya4, Tatsuhiko Tsunoda4, Kenjiro Kosaki5, Tomohiro Kumada2, Minoru Shibata2, Tatsuya Fujii2.   

Abstract

Cutis laxa (CL) syndromes are connective tissue disorders characterized by redundant, sagging, inelastic and wrinkled skin, with organ involvement. Here, we describe a patient with ALDH18A1-related CL who developed cyclic vomiting. The patient was a 12-year-old boy who presented with poor postnatal growth, hypotonia, short stature, joint hyperlaxity, microcephaly, strabismus, bilateral cataracts, facial dysmorphism and severe mental retardation. Bone radiographs showed osteopenia and osteoporosis, and magnetic resonance angiography showed marked kinking and tortuosity of the brain vessels. These findings were clinically compatible with ALDH18A1-related CL. Molecular analysis revealed a de novo heterozygous mutation (p.R138Q) in ALDH18A1. No mutations were found in PYCR1 gene. The patient developed cyclic vomiting with decreased blood levels of ornithine, citrulline, arginine and proline without hyperammonemia and other hypoaminoacidemias were also found. ALDH18A1 encodes Δ(1)-pyrroline-5-carboxylate synthase, which is related to the biosynthesis of ornithine, citrulline, arginine, and proline. Cyclic vomiting has never been reported in other ALDH18A1-related CL patients. This is the first case report of ALDH18A1-related CL with cyclic vomiting associated with amino acid abnormalities.
Copyright © 2016 The Japanese Society of Child Neurology. Published by Elsevier B.V. All rights reserved.

Entities:  

Keywords:  ALDH18A1; Cutis laxa syndrome; Cyclic vomiting; P5CS; R138

Mesh:

Substances:

Year:  2016        PMID: 26829900     DOI: 10.1016/j.braindev.2016.01.003

Source DB:  PubMed          Journal:  Brain Dev        ISSN: 0387-7604            Impact factor:   1.961


  5 in total

1.  Novel mutations in the ALDH18A1 gene in complicated hereditary spastic paraplegia with cerebellar ataxia and cognitive impairment.

Authors:  Kishin Koh; Hiroyuki Ishiura; Minako Beppu; Haruo Shimazaki; Yuta Ichinose; Jun Mitsui; Satoshi Kuwabara; Shoji Tsuji; Yoshihisa Takiyama
Journal:  J Hum Genet       Date:  2018-06-18       Impact factor: 3.172

2.  Autosomal dominant cutis laxa with progeroid features due to a novel, de novo mutation in ALDH18A1.

Authors:  Priya T Bhola; Taila Hartley; Eric Bareke; Kym M Boycott; Sarah M Nikkel; David A Dyment
Journal:  J Hum Genet       Date:  2017-02-23       Impact factor: 3.172

3.  SPG9A with the new occurrence of an ALDH18A1 mutation in a CMT1A family with PMP22 duplication: case report.

Authors:  Kishin Koh; Ryusuke Takaki; Hiroyuki Ishiura; Shoji Tsuji; Yoshihisa Takiyama
Journal:  BMC Neurol       Date:  2021-02-11       Impact factor: 2.474

Review 4.  The genetics of mitochondrial disease: dissecting mitochondrial pathology using multi-omic pipelines.

Authors:  Charlotte L Alston; Sarah L Stenton; Gavin Hudson; Holger Prokisch; Robert W Taylor
Journal:  J Pathol       Date:  2021-03-26       Impact factor: 9.883

5.  PYCR2 Mutations cause a lethal syndrome of microcephaly and failure to thrive.

Authors:  Maha S Zaki; Gifty Bhat; Tipu Sultan; Mahmoud Issa; Hea-Jin Jung; Esra Dikoglu; Laila Selim; Imam G Mahmoud; Mohamed S Abdel-Hamid; Ghada Abdel-Salam; Isaac Marin-Valencia; Joseph G Gleeson
Journal:  Ann Neurol       Date:  2016-06-01       Impact factor: 10.422

  5 in total

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