Zobrazeno 1 - 10
of 97
pro vyhledávání: '"Dania Al Jaroudi"'
Publikováno v:
Clinical Case Reports, Vol 12, Iss 11, Pp n/a-n/a (2024)
Key clinical message Perrault syndrome (PRLTS) is an uncommon hereditary condition distinguished by ovarian failure in females and sensorineural hearing loss. Infertility can be the presenting problem for a serious disease. History and physical exami
Externí odkaz:
https://doaj.org/article/16e56d1399f44acab3eeb6511914f04c
Autor:
Shuruq Alkhalaf, Nadeef Alqahtani, Amani AbuAlnaja, Saud Alhassoun, Alexandra Alkhatir, Dania Al-Jaroudi
Publikováno v:
The Journal of Medicine, Law & Public Health, Vol 3, Iss 4 (2023)
Introduction: This study assessed the prevalence of congenital malformation among neonates born after using progesterone for luteal support in patients undergoing IVF and ICSI cycles. Methods: This retrospective cohort study was conducted in the
Externí odkaz:
https://doaj.org/article/f0d7feecbfa84dc3a1c176a48be5e685
Publikováno v:
Human Vaccines & Immunotherapeutics, Vol 17, Iss 2, Pp 377-380 (2021)
Background: The infection of rubella in pregnancy is worrisome due to the fact that it causes miscarriages, congenital defects, and Congenital Rubella Syndrome (CRS). The purpose of this study was to determine the status of Rubella IgG antibody level
Externí odkaz:
https://doaj.org/article/8dfa9833deec4cc387f05f3016f7e65e
Autor:
Munazzah Rafique, Dania Al Jaroudi
Publikováno v:
Pakistan Journal of Medical Research, Vol 61, Iss 1 (2022)
Background: Disorder in sex development (DSD) refers to a variety of diagnoses in which the development of chromosomal make-up, gonadal development, or anatomical development is abnormal. The most prevalent XY, DSD diagnosis is Complete Androgen Inse
Externí odkaz:
https://doaj.org/article/c40c37b8298b4e04b92bbf2744a667a7
Publikováno v:
Clinical Case Reports, Vol 7, Iss 6, Pp 1238-1241 (2019)
Abstract We report a patient with primary infertility and clinical manifestation of premature ovarian insufficiency (POI) who upon investigation was found to have streak ovaries, and genetic testing revealed Trisomy X (47, XXX). Therefore, we suggest
Externí odkaz:
https://doaj.org/article/2ef56d9a467e4e6fbca97107c9e8e736
Autor:
Ayah Hijazi, Dania Al-Jaroudi
Publikováno v:
Case Reports in Women's Health, Vol 15, Iss C, Pp 8-10 (2017)
Background: Severe vulvar edema is a rare entity occurring with ovarian hyperstimulation syndrome. This edema can be incapacitating; causing pain and limited patient mobility. With the usual conservative approach, vulvar edema can take several days t
Externí odkaz:
https://doaj.org/article/c236bed9e88e4c31b31689078c111d3a
Publikováno v:
Case Reports in Women's Health, Vol 20, Iss , Pp - (2018)
Background: Acute abdomen in pregnancy is a unique clinical challenge. We report a rare case of hydrosalpinx presenting as acute abdomen in the third trimester of pregnancy in the absence of infection and hormonal treatment. Case: A 38-year-old Cauca
Externí odkaz:
https://doaj.org/article/682b921f5814495abe3bbaaf32e66b30
