Zobrazeno 1 - 10
of 12
pro vyhledávání: '"renal agenezi"'
Publikováno v:
Sakarya Tıp Dergisi, Vol 12, Iss 3, Pp 536-543 (2022)
Objective: The aim of this study is to report our experience on the management of seminal vesicle cyst which is an exceedingly rare acquired or congenital pathology. Materials and Methods: A retrospective chart review was conducted on seven patients
Externí odkaz:
https://doaj.org/article/0fed7fdd5cae4a7bbf7faa11fa93d44a
Publikováno v:
Cukurova Medical Journal, Vol 44, Iss 4, Pp 1546-1548 (2019)
Externí odkaz:
https://doaj.org/article/44cd6b96d84249bd9d811e02f9c7652e
Publikováno v:
Volume: 12, Issue: 3 536-543
Sakarya Tıp Dergisi
Sakarya Medical Journal
Sakarya Tıp Dergisi
Sakarya Medical Journal
Objective: The aim of this study is to report our experience on the management of seminal vesicle cyst which is an exceedingly rare acquired or congenital pathology. Materials and Methods: A retrospective chart review was conducted on seven patients
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=tubitakulakb::4c16fe8a9685b5bed108664b30842d9a
https://dergipark.org.tr/tr/pub/smj/issue/72629/1104876
https://dergipark.org.tr/tr/pub/smj/issue/72629/1104876
Publikováno v:
Volume: 6, Issue: 2 113-117
Kocaeli Üniversitesi Sağlık Bilimleri Dergisi
Kocaeli Üniversitesi Sağlık Bilimleri Dergisi
Objective: Renal agenesis and Multicystic Dysplastic Kidney (MCDK) are among the developmental kidney defects. There is only one kidney that functions in both diseases. In these studies, both diseases were examined separately and their long term resu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d1fe3516ab52cc1a80998b01fcb79c8
https://doi.org/10.30934/kusbed.643654
https://doi.org/10.30934/kusbed.643654
Publikováno v:
Volume: 16, Issue: 3 246-248
Türkiye Çocuk Hastalıkları Dergisi
Türkiye Çocuk Hastalıkları Dergisi
Bartter Syndrome (BS) is a hereditary condition characterized by polyuria, renal salt wasting, and hypokalemic metabolic alkalosis with high serum renin and aldosterone levels. Patients with BS usually have symptoms in the first two years of life, bu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::72af6093ab2dc0a5e4d841342f73da2a
https://dergipark.org.tr/tr/pub/tchd/issue/69917/940636
https://dergipark.org.tr/tr/pub/tchd/issue/69917/940636
Publikováno v:
Cukurova Medical Journal, Vol 44, Iss 4, Pp 1546-1548 (2019)
Nöral tüp defektleri (NTD) anormal nörilasyon nedeniyle oluşan, prenatal ve postnatal dönemde önemli tıbbi sorunlara yol açabilen, ölümle sonuçlanabilen, finansal ve sosyal boyutları da olan bir konjenital malformasyon grubudur1. Meningom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::e0fd64b2e38db92ffa9324aeac7a1076
https://dergipark.org.tr/tr/pub/cumj/issue/42408/573041?publisher=cu
https://dergipark.org.tr/tr/pub/cumj/issue/42408/573041?publisher=cu
Publikováno v:
Volume: 44, Issue: 4 1546-1548
Cukurova Medical Journal
Cukurova Medical Journal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::64685aa25889fb05905c90a4c70e55e0
https://dergipark.org.tr/tr/pub/cumj/issue/42408/573041
https://dergipark.org.tr/tr/pub/cumj/issue/42408/573041
Autor:
Abdulhamit Tuten, Mehmet Burak Mutlu, Handan Hakyemez Toptan, Tulin Gokmen Yildirim, Nilgün Karadağ, Gülsen Akay, Güner Karatekin
Publikováno v:
Volume: 47, Issue: 4 129-132
Zeynep Kamil Tıp Bülteni
Zeynep Kamil Tıp Bülteni
Turner syndrome is a genetic disorder causedby loss or structural disorders of X chromosome.A significant number of cases result with abortion.Clinical symptoms are not always apparent in thenewborn period. Therefore it could be diagnosed inlater yea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d02737338eeca0a3edff9916691348c4
https://dergipark.org.tr/tr/pub/zktipb/issue/27383/237205
https://dergipark.org.tr/tr/pub/zktipb/issue/27383/237205
Autor:
İLHAN, Özkan, ÖZER, Esra Arun, ALKAN, Senem, AKBAY, Sinem, KANAR, Berat, MEMUR, Şeyma, SÜTÇÜOĞLU, Sümer
Publikováno v:
Volume: 2, Issue: 3 47-49
Muğla Sıtkı Koçman Üniversitesi Tıp Dergisi
Muğla Sıtkı Koçman Üniversitesi Tıp Dergisi
Potter sendromu, iki taraflı böbrek yokluğu, oligohidramniyoz, akciğer hipoplazisi, ekstremite anomalileri ve tipik yüz görünümü ile karakterize nadir görülen bir hastalıktır. Potter sendromundaki anomaliler oligohidroamniyoz nedeniyle o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=tubitakulakb::484665c838000ed1294861abe7fee827
https://dergipark.org.tr/tr/pub/muskutd/issue/34650/382846
https://dergipark.org.tr/tr/pub/muskutd/issue/34650/382846
Publikováno v:
Volume: 1, Issue: 3 31-34
Kocaeli Tıp Dergisi
Kocaeli Tıp Dergisi
Uterus didelphys with blind hemivagina and ipsilateral renal agenesis is a very rare anomaly and may be found in a female with normal menstrual periods.We report two cases with a double uterus, unilateral vaginal obstruction and ipsilateral renal age
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=tubitakulakb::ba7a037e6ef0b88efa8262d5ccafb9b6
https://dergipark.org.tr/tr/pub/kotder/issue/38572/447537
https://dergipark.org.tr/tr/pub/kotder/issue/38572/447537