Osteogenesis imperfecta/Ehlers-Danlos overlap syndrome (COL1-related disorder) and pregnancy

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00098892%3A_____%2F22%3A10157547" target="_blank" >RIV/00098892:_____/22:10157547 - isvavai.cz</a>

Nalezeny alternativní kódy

RIV/61989592:15110/22:73616685

Výsledek na webu

<a href="https://www.cs-gynekologie.cz/en/journals/czech-gynaecology/2022-6-6/osteogenesis-imperfecta-ehlers-danlosuv-syndrom-col1-asociovane-onemocneni-v-tehotenstvi-133024" target="_blank" >https://www.cs-gynekologie.cz/en/journals/czech-gynaecology/2022-6-6/osteogenesis-imperfecta-ehlers-danlosuv-syndrom-col1-asociovane-onemocneni-v-tehotenstvi-133024</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.48095/cccg2022396" target="_blank" >10.48095/cccg2022396</a>

Jazyk výsledku

angličtina

Název v původním jazyce

Osteogenesis imperfecta/Ehlers-Danlos overlap syndrome (COL1-related disorder) and pregnancy

Popis výsledku v původním jazyce

Ehlers-Danlos syndrome is in a group of connective tissue disorders that can result in a range of complications during pregnancy. Clinical manifestations include skin hyperextensibility, atrophic scarring, poor wound healing, hyperflexibility or higher risk of organ ruptures (uterine rupture, aortal dissection). The combination of Ehlers-Danlos syndrome and osteogenesis imperfecta is very rare (< 1/1,000,000 according to Orphanet). We are presenting a case of woman with osteogenesis imperfecta/Ehlers-Danlos overlap syndrome and her pregnancy complicated by aortal dilatation. Our case has attempted to highlight the potential obstetric complications and to attract the attention of clinical physicians to the rare but extremely dangerous syndrome.

Název v anglickém jazyce

Osteogenesis imperfecta/Ehlers-Danlos overlap syndrome (COL1-related disorder) and pregnancy

Popis výsledku anglicky

Ehlers-Danlos syndrome is in a group of connective tissue disorders that can result in a range of complications during pregnancy. Clinical manifestations include skin hyperextensibility, atrophic scarring, poor wound healing, hyperflexibility or higher risk of organ ruptures (uterine rupture, aortal dissection). The combination of Ehlers-Danlos syndrome and osteogenesis imperfecta is very rare (< 1/1,000,000 according to Orphanet). We are presenting a case of woman with osteogenesis imperfecta/Ehlers-Danlos overlap syndrome and her pregnancy complicated by aortal dilatation. Our case has attempted to highlight the potential obstetric complications and to attract the attention of clinical physicians to the rare but extremely dangerous syndrome.

Druh

J_imp - Článek v periodiku v databázi Web of Science

CEP obor

—

OECD FORD obor

30214 - Obstetrics and gynaecology

Projekt

—

Návaznosti

I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Rok uplatnění

2022

Kód důvěrnosti údajů

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Název periodika

Česká gynekologie

ISSN

1210-7832

e-ISSN

1805-4455

Svazek periodika

87

Číslo periodika v rámci svazku

6

Stát vydavatele periodika

CZ - Česká republika

Počet stran výsledku

5

Strana od-do

396-400

Kód UT WoS článku

001015221400001

EID výsledku v databázi Scopus

2-s2.0-85144476934