Pregled bibliografske jedinice broj: 1071429
Meckel Gruber Syndrome: a rare and lethal anomaly
Meckel Gruber Syndrome: a rare and lethal anomaly // Clinical Journal of Obstetrics and Gynecology, 2 (2019), 133-134 doi:10, 29328/journal.cjog.1001035 (međunarodna recenzija, prikaz, stručni)
CROSBI ID: 1071429 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Meckel Gruber Syndrome: a rare and lethal anomaly
Autori
Žegarac, Žana ; Duić, Željko ; Bojanić, Katarina
Izvornik
Clinical Journal of Obstetrics and Gynecology (2640-2890) 2
(2019);
133-134
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, prikaz, stručni
Ključne riječi
fetus ; meckel gruger syndrome ; lethal anomaly
Sažetak
We present our case of the rare Meckel-Gruber syndrome, diagnosed prenatally at 18 weeks gestation. Characteristic findings include occipital encephalocele, polycistic kidneya and post axial polydactyly. The mean gestation age at diagnosis is 14 weeks.MGS is lethal disorder. Most infants are stillborn or die within a few hours or daya following birth. As MGS has a high risk of recurrence, genetic counseling should be provided. Early diagnosis isd importante for the timely consultation of affected couples regarding their decision of pregnancy termination
Izvorni jezik
Engleski
Znanstvena područja
Biotehnologija u biomedicini (prirodno područje, biomedicina i zdravstvo, biotehničko područje)
POVEZANOST RADA
Ustanove:
Klinička bolnica "Merkur",
Medicinski fakultet, Zagreb
Profili:
Željko Duić
(autor)
