Cargando…
Presymptomatic genetic analysis during pregnancy for vascular type Ehlers–Danlos syndrome
The vascular type of Ehlers–Danlos syndrome (EDS), EDS type IV (Online Mendelian Inheritance in Man [MIM] #130050) is characterized by thin, translucent skin, easy bruising, and arterial, intestinal, and/or uterine fragility during pregnancy, which may lead to sudden death. It is an autosomal domina...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4069127/ https://www.ncbi.nlm.nih.gov/pubmed/24971038 http://dx.doi.org/10.2147/IMCRJ.S59879 |
_version_ | 1782322514202984448 |
---|---|
author | Naing, Banyar Than Watanabe, Atsushi Tanigaki, Shinji Ono, Masae Iwashita, Mitsutoshi Shimada, Takashi |
author_facet | Naing, Banyar Than Watanabe, Atsushi Tanigaki, Shinji Ono, Masae Iwashita, Mitsutoshi Shimada, Takashi |
author_sort | Naing, Banyar Than |
collection | PubMed |
description | The vascular type of Ehlers–Danlos syndrome (EDS), EDS type IV (Online Mendelian Inheritance in Man [MIM] #130050) is characterized by thin, translucent skin, easy bruising, and arterial, intestinal, and/or uterine fragility during pregnancy, which may lead to sudden death. It is an autosomal dominant inherited disorder caused by type III procollagen gene (COL3A1: MIM #120180) mutations. Approximately 50% of the COL3A1 mutations are inherited from an affected parent, and 50% are de novo mutations. Each child of an affected individual has a 50% chance of inheriting the mutation and developing the disorder. Pregnant women with vascular EDS are at an increased risk of uterine and arterial rupture during the peripartum period, with high maternal morbidity and mortality rates. We report the first case of an asymptomatic 35-year-old woman at a risk of complications of vascular EDS who underwent presymptomatic evaluation during pregnancy. The sequencing results of both her brother and mother had a one-base-pair deletion, resulting in Glutamate at position 730 changing to Lysine and causing a frame shift and premature termination codon at 61 amino acids from the mutation position (p. Glu730Lysfs*61) on exon 32 of COL3A1. This deletion caused frameshift, leading to a premature termination codon (TAG) at 181 nucleotides downstream in exon 35, which could not be detected by previous total RNA (ribonucleic acid) method. Thus, she was at risk of complications of vascular EDS, and diagnostic testing was employed at 8 weeks of pregnancy to minimize the risk of developing vascular EDS-related complications. The negative presymptomatic diagnostic result allowed the patient to choose normal delivery at term. Vascular EDS is a serious disorder, with high mortality, especially in high-risk women with vascular EDS during pregnancy. The presymptomatic genetic testing of vascular EDS during pregnancy for a high-risk family can help with the early establishment of preventive measures. |
format | Online Article Text |
id | pubmed-4069127 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-40691272014-06-26 Presymptomatic genetic analysis during pregnancy for vascular type Ehlers–Danlos syndrome Naing, Banyar Than Watanabe, Atsushi Tanigaki, Shinji Ono, Masae Iwashita, Mitsutoshi Shimada, Takashi Int Med Case Rep J Case Report The vascular type of Ehlers–Danlos syndrome (EDS), EDS type IV (Online Mendelian Inheritance in Man [MIM] #130050) is characterized by thin, translucent skin, easy bruising, and arterial, intestinal, and/or uterine fragility during pregnancy, which may lead to sudden death. It is an autosomal dominant inherited disorder caused by type III procollagen gene (COL3A1: MIM #120180) mutations. Approximately 50% of the COL3A1 mutations are inherited from an affected parent, and 50% are de novo mutations. Each child of an affected individual has a 50% chance of inheriting the mutation and developing the disorder. Pregnant women with vascular EDS are at an increased risk of uterine and arterial rupture during the peripartum period, with high maternal morbidity and mortality rates. We report the first case of an asymptomatic 35-year-old woman at a risk of complications of vascular EDS who underwent presymptomatic evaluation during pregnancy. The sequencing results of both her brother and mother had a one-base-pair deletion, resulting in Glutamate at position 730 changing to Lysine and causing a frame shift and premature termination codon at 61 amino acids from the mutation position (p. Glu730Lysfs*61) on exon 32 of COL3A1. This deletion caused frameshift, leading to a premature termination codon (TAG) at 181 nucleotides downstream in exon 35, which could not be detected by previous total RNA (ribonucleic acid) method. Thus, she was at risk of complications of vascular EDS, and diagnostic testing was employed at 8 weeks of pregnancy to minimize the risk of developing vascular EDS-related complications. The negative presymptomatic diagnostic result allowed the patient to choose normal delivery at term. Vascular EDS is a serious disorder, with high mortality, especially in high-risk women with vascular EDS during pregnancy. The presymptomatic genetic testing of vascular EDS during pregnancy for a high-risk family can help with the early establishment of preventive measures. Dove Medical Press 2014-06-19 /pmc/articles/PMC4069127/ /pubmed/24971038 http://dx.doi.org/10.2147/IMCRJ.S59879 Text en © 2014 Naing et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Case Report Naing, Banyar Than Watanabe, Atsushi Tanigaki, Shinji Ono, Masae Iwashita, Mitsutoshi Shimada, Takashi Presymptomatic genetic analysis during pregnancy for vascular type Ehlers–Danlos syndrome |
title | Presymptomatic genetic analysis during pregnancy for vascular type Ehlers–Danlos syndrome |
title_full | Presymptomatic genetic analysis during pregnancy for vascular type Ehlers–Danlos syndrome |
title_fullStr | Presymptomatic genetic analysis during pregnancy for vascular type Ehlers–Danlos syndrome |
title_full_unstemmed | Presymptomatic genetic analysis during pregnancy for vascular type Ehlers–Danlos syndrome |
title_short | Presymptomatic genetic analysis during pregnancy for vascular type Ehlers–Danlos syndrome |
title_sort | presymptomatic genetic analysis during pregnancy for vascular type ehlers–danlos syndrome |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4069127/ https://www.ncbi.nlm.nih.gov/pubmed/24971038 http://dx.doi.org/10.2147/IMCRJ.S59879 |
work_keys_str_mv | AT naingbanyarthan presymptomaticgeneticanalysisduringpregnancyforvasculartypeehlersdanlossyndrome AT watanabeatsushi presymptomaticgeneticanalysisduringpregnancyforvasculartypeehlersdanlossyndrome AT tanigakishinji presymptomaticgeneticanalysisduringpregnancyforvasculartypeehlersdanlossyndrome AT onomasae presymptomaticgeneticanalysisduringpregnancyforvasculartypeehlersdanlossyndrome AT iwashitamitsutoshi presymptomaticgeneticanalysisduringpregnancyforvasculartypeehlersdanlossyndrome AT shimadatakashi presymptomaticgeneticanalysisduringpregnancyforvasculartypeehlersdanlossyndrome |