Both a frameshift and a missense mutation of the STRA6 gene observed in an infant with the Matthew-Wood syndrome
| العنوان: | Both a frameshift and a missense mutation of the STRA6 gene observed in an infant with the Matthew-Wood syndrome |
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| المؤلفون: | Sadowski, Samantha, Chassaing, Nicolas, Gaj, Zuzanna, Czichos, Ewa, Wilczynski, Jan, Nowakowska, Dorota |
| المساهمون: | Medical University of Łódź (MUL), Unité différenciation épidermique et auto-immunité rhumatoïde (UDEAR), Université Toulouse III - Paul Sabatier (UT3), Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-Institut National de la Santé et de la Recherche Médicale (INSERM), Hôpital Purpan [Toulouse], CHU Toulouse [Toulouse], Polish Mother’s Memorial Hospital Research Institute [Lodz] (ICZMP), Duchess Anna Mazowiecka Public Teaching Hospital [Warsaw] |
| المصدر: | Birth Defects Research Birth Defects Research, Wiley, 2017, 109 (4), pp.251-253. ⟨10.1002/bdra.23465⟩ |
| سنة النشر: | 2015 |
| مصطلحات موضوعية: | MESH: Lung Diseases / diagnosis, Lung Diseases, Male, MESH: Respiratory Insufficiency / genetics, MESH: Fatal Outcome, MESH: Gene Expression, MESH: Lung / pathology, Inheritance Patterns, Mutation, Missense, Gene Expression, MESH: Membrane Proteins / genetics, MESH: Anophthalmos / diagnosis, STRA6 gene mutations, MESH: Microphthalmos / diagnosis, MESH: Pregnancy, Fatal Outcome, [SDV.MHEP.MI]Life Sciences [q-bio]/Human health and pathology/Infectious diseases, Pregnancy, anophthalmia, Humans, Microphthalmos, Abnormalities, Multiple, MESH: Lung Diseases / pathology, Frameshift Mutation, Lung, MESH: Anophthalmos / pathology, MESH: Microphthalmos / pathology, MESH: Respiratory Insufficiency / diagnosis, MESH: Humans, MESH: Lung Diseases / genetics, MESH: Frameshift Mutation, MESH: Lung / abnormalities, Anophthalmos, Infant, Membrane Proteins, MESH: Anophthalmos / genetics, MESH: Abnormalities, Multiple / genetics, MESH: Microphthalmos / genetics, MESH: Infant, MESH: Male, MESH: Mutation, Missense, MESH: Abnormalities, Multiple / diagnosis, MESH: Respiratory Insufficiency / pathology, Matthew-Wood syndrome, MESH: Abnormalities, Multiple / pathology, Female, MESH: Inheritance Patterns, Respiratory Insufficiency, MESH: Female |
| الوصف: | International audience; Background: The Matthew-Wood syndrome is associated with mutations of the STRA6 gene. It combines a pulmonary agenesis/hypoplasia; microphthalmia/anophthalmia; congenital cardiac, digestive, and urogenital malformations; and diaphragmatic defects. Case: A 23-year-old nulliparous woman was referred to our center after a fetal ultrasound examination at 26 weeks of pregnancy revealed an abnormal head shape, a heart malformation, multiple cysts in both kidneys, and dilated ureters. A male baby (46, XY; 3600g; Apgar score 1) was delivered at 38 weeks of gestation and died 1 hr later due to respiratory failure. The diagnosis of Matthew-Wood syndrome was suspected given the association of bilateral anophthalmia, agenesis of the left lung, and heart and kidney defects. It was confirmed by the identification of two deleterious mutations of the STRA6 gene. Results: The child was a compound heterozygote for two previously reported mutations, a paternally inherited missense mutation (c.878C>T [p.Pro293Leu] and a maternally inherited frameshift mutation (c.50_52delACTinsCC [p. Asp17Alafs*55]), producing a premature stop codon. Conclusion: The diagnosis of Matthew-Wood syndrome should be considered in all fetuses with microphthalmia/anophthalmia. It requires an extensive ultrasound/MRI examination of the lung, heart, and diaphragm. Birth Defects Research 109:251-253, 2017. © 2017 Wiley Periodicals, Inc. |
| تدمد: | 2472-1727 |
| الوصول الحر: | https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::800f77e7ed4d0e01ed307d6c52a1d818Test https://pubmed.ncbi.nlm.nih.gov/28398665Test |
| رقم الانضمام: | edsair.pmid.dedup....800f77e7ed4d0e01ed307d6c52a1d818 |
| قاعدة البيانات: | OpenAIRE |
| تدمد: | 24721727 |
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