prikaz prve stranice dokumenta Meckel Gruber Syndrome
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Meckel Gruber Syndrome
Gazzetta Medica Italiana Archivo per le Scienze Mediche, 176 (2017), 7-8; 424-425. https://doi.org/10.23736/S0393-3660.16.03395-7
Sabolović Rudman, Senka; Djaković, Ivka; Košec, Vesna

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Sabolović Rudman, S., Djaković, I. i Košec, V. (2017). Meckel Gruber Syndrome. Gazzetta Medica Italiana Archivo per le Scienze Mediche, 176. (7-8), 424-425. doi: 10.23736/S0393-3660.16.03395-7

Sabolović Rudman, Senka, et al. "Meckel Gruber Syndrome." Gazzetta Medica Italiana Archivo per le Scienze Mediche, vol. 176, br. 7-8, 2017, str. 424-425. https://doi.org/10.23736/S0393-3660.16.03395-7

Sabolović Rudman, Senka, Ivka Djaković i Vesna Košec. "Meckel Gruber Syndrome." Gazzetta Medica Italiana Archivo per le Scienze Mediche 176, br. 7-8 (2017): 424-425. https://doi.org/10.23736/S0393-3660.16.03395-7

Sabolović Rudman, S., Djaković, I. i Košec, V. (2017) 'Meckel Gruber Syndrome', Gazzetta Medica Italiana Archivo per le Scienze Mediche, 176(7-8), str. 424-425. doi: 10.23736/S0393-3660.16.03395-7

Sabolović Rudman S, Djaković I, Košec V. Meckel Gruber Syndrome. Gazzetta Medica Italiana Archivo per le Scienze Mediche [Internet]. 2017. [pristupljeno 22.01.2025.];176(7-8):424-425. doi: 10.23736/S0393-3660.16.03395-7

S. Sabolović Rudman, I. Djaković i V. Košec, "Meckel Gruber Syndrome", Gazzetta Medica Italiana Archivo per le Scienze Mediche, vol. 176, br. 7-8, str. 424-425, 2017. [Online]. Dostupno na: https://urn.nsk.hr/urn:nbn:hr:220:014324. [Citirano: 22.01.2025.]

Za citiranje koristite ovu mrežnu adresu: https://urn.nsk.hr/urn:nbn:hr:220:014324
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Podaci o radu
Naslov (engleski)Meckel Gruber Syndrome
AutorSenka Sabolović Rudman
AutorIvka Djaković
AutorVesna Košec
Autorova ustanova(Klinički bolnički centar Sestre milosrdnice)
Znanstveno / umjetničko
područje, polje i grana		BIOMEDICINA I ZDRAVSTVO
Kliničke medicinske znanosti
Ginekologija i opstetricija
Sažetak (engleski)
Meckel Gruber Syndrome is an autosomal recessive syndrome characterized by a wide variety of systemic malformations. It is a rare syndrome, the worldwide incidence varies from 1 in 13250 to 1 in 140000 live births. There is great diversity of malformations in this syndrome and it is almost always lethal. We present a case of a patient that had two inducted abortions for Meckel Gruber syndrome. The diagnosis was confirmed pathohystologicaly. She also had two normal term pregnancies. Adequate antenatal care results in early diagnosis of Meckel Gruber syndrome and prompt termination of pregnancy is required.
Ključne riječi (engleski)
Jezikengleski
Vrsta publikacijeOstalo - Prikaz, pregled, osvrt
Status objaveObjavljen
Vrsta recenzijeRecenziran
Verzija publikacijeObjavljena verzija rada (izdavačev PDF)
Naslov časopisaGazzetta Medica Italiana Archivo per le Scienze Mediche
Brojčani podacivol. 176, br. 7-8, str. 424-425
p-ISSN0393-3660
e-ISSN1827-1812
DOIhttps://doi.org/10.23736/S0393-3660.16.03395-7
URN:NBNurn:nbn:hr:220:014324
Datum objave publikacije2017
URL dokumentahttps://www.minervamedica.it/it/riviste/gazzetta-medica-italiana/articolo.php?cod=R22Y2017N07A0424
Vrsta resursaTekst
Prava pristupaInstitucijski pristup
Uvjeti korištenjaIkona licence Zaštićeno autorskim pravom.
Datum i vrijeme pohrane2025-01-13 12:25:50