| Literature DB >> 26829900 |
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.Entities:
Keywords: ALDH18A1; Cutis laxa syndrome; Cyclic vomiting; P5CS; R138
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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