Zobrazeno 1 - 10
of 94
pro vyhledávání: '"Yen-Ni Chen"'
Publikováno v:
Taiwanese Journal of Obstetrics & Gynecology, Vol 62, Iss 2, Pp 334-335 (2023)
Objectives: The main objectives of this case report are to discuss prenatal ultrasound findings of congenital radioulnar synostosis and to review the literature. Case report: A patient was diagnosed with congenital radioulnar synostosis at eight mont
Externí odkaz:
https://doaj.org/article/a403edf9563f43eb839977333069e114
Autor:
Chih-Ping Chen, Shu-Yuan Chang, Yen-Ni Chen, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Shih-Ting Lai, Tzu-Yun Chuang, Chien-Wen Yang, Li-Feng Chen, Wayseen Wang
Publikováno v:
Taiwanese Journal of Obstetrics & Gynecology, Vol 57, Iss 5, Pp 739-744 (2018)
Objective: We present prenatal diagnosis of a familial 1q21.1-q21.2 microdeletion in a fetus with polydactyly of left foot on prenatal ultrasound. Case report: A 30-year-old, gravida 2, para 1, woman underwent amniocentesis at 22 weeks of gestation b
Externí odkaz:
https://doaj.org/article/8ae57f30b6b749df9b942fb1f97d1c03
Autor:
Chih-Ping Chen, Ming Chen, Chia-Hsun Wu, Chen-Ju Lin, Schu-Rern Chern, Peih-Shan Wu, Yen-Ni Chen, Shin-Wen Chen, Shun-Ping Chang, Li-Feng Chen, Wayseen Wang
Publikováno v:
Taiwanese Journal of Obstetrics & Gynecology, Vol 56, Iss 4, Pp 554-557 (2017)
Objective: We present prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome (sSMC) derived from chromosome 21q11.2-q21.1, and we review the literature of an sSMC(21) with a duplication
Externí odkaz:
https://doaj.org/article/6afd18874dce4177aaf9abd69a32bf5a
Autor:
Chih-Ping Chen, Chen-Ju Lin, Yen-Ni Chen, Schu-Rern Chern, Shin-Wen Chen, Shih-Ting Lai, Peih-Shan Wu, Li-Feng Chen, Wayseen Wang
Publikováno v:
Taiwanese Journal of Obstetrics & Gynecology, Vol 56, Iss 3, Pp 398-401 (2017)
Objective: We present prenatal diagnosis and molecular genetic characterization of a de novo interstitial deletion of 2q (2q31.1-q32.1) and discuss the genotype–phenotype correlation. Case report: A 34-year-old, primigravid woman was referred to th
Externí odkaz:
https://doaj.org/article/fe89e82caee1478bbddaca1c91b90de1
Autor:
Chih-Ping Chen, Tsang-Ming Ko, Liang-Kai Wang, Shuan-Pei Lin, Schu-Rern Chern, Peih-Shan Wu, Yen-Ni Chen, Shin-Wen Chen, Chien-Wen Yang, Dai-Dyi Town, Meng-Shan Lee, Wayseen Wang
Publikováno v:
Taiwanese Journal of Obstetrics & Gynecology, Vol 56, Iss 2, Pp 264-267 (2017)
Externí odkaz:
https://doaj.org/article/8a4fa858a4934e0db444f5ab7c882d8a
Autor:
Chih-Ping Chen, Schu-Rern Chern, Yen-Ni Chen, Shin-Wen Chen, Peih-Shan Wu, Chien-Wen Yang, Chen-Chi Lee, Meng-Shan Lee, Chen-Wen Pan, Wayseen Wang
Publikováno v:
Taiwanese Journal of Obstetrics & Gynecology, Vol 56, Iss 2, Pp 217-223 (2017)
Objective: We present prenatal diagnosis and molecular cytogenetic characterization of concomitant familial small supernumerary marker chromosome 4 [sSMC(4)] derived from 4q11.1–q12 and q13.2, and 5q13.2 microdeletion with no apparent phenotypic ab
Externí odkaz:
https://doaj.org/article/6b48b17a80e94ecfb49813baed60ab3f
Autor:
Chih-Ping Chen, Chen-Ju Lin, Schu-Rern Chern, Peih-Shan Wu, Yen-Ni Chen, Shin-Wen Chen, Chen-Wen Pan, Chien-Wen Yang, Wayseen Wang
Publikováno v:
Taiwanese Journal of Obstetrics & Gynecology, Vol 56, Iss 2, Pp 238-242 (2017)
Objective: We present prenatal diagnosis of low-level mosaic trisomy 12. Case Report: A 40-year-old woman underwent amniocentesis at 18 weeks of gestation because of advanced maternal age, which revealed a karyotype of 47,XX,+12[5]/46,XX[24] consiste
Externí odkaz:
https://doaj.org/article/35fa87deb7584d14b30be685084b3280
Autor:
Chih-Ping Chen, Kuo-Gon Wang, Hsu-Kuang Huang, Cheng-Ran Peng, Schu-Rern Chern, Peih-Shan Wu, Yen-Ni Chen, Shin-Wen Chen, Chen-Chi Lee, Wayseen Wang
Publikováno v:
Taiwanese Journal of Obstetrics & Gynecology, Vol 56, Iss 2, Pp 230-233 (2017)
Objective: We present cytogenetic and molecular cytogenetic diagnoses of mosaic deletion of chromosome 15q11.1-q11.2 in a fetus with diffuse lymphangiomatosis. Case Report: A 33-year-old woman underwent amniocentesis at 22 weeks of gestation because
Externí odkaz:
https://doaj.org/article/a6d6e159c9d947bf8717cccfc6603f1c
Prenatal Ultrasound Evaluation and Outcome of Pregnancy with Fetal Cystic Hygromas and Lymphangiomas
Publikováno v:
Journal of Medical Ultrasound, Vol 25, Iss 1, Pp 12-15 (2017)
Cystic hygroma is a type of lymphangioma, which is a vascular anomaly associated with lymphatic malformations and formed by fluid accumulation mainly located at the cervicofacial and axillary regions. Cystic hygroma is mostly located in the neck (75%
Externí odkaz:
https://doaj.org/article/9407119c29b54e33b7c9ccfc6b7a357a
Autor:
Chih-Ping Chen, Shuan-Pei Lin, Chung-Lin Lee, Schu-Rern Chern, Peih-Shan Wu, Yen-Ni Chen, Shin-Wen Chen, Wayseen Wang
Publikováno v:
Taiwanese Journal of Obstetrics & Gynecology, Vol 56, Iss 1, Pp 93-97 (2017)
Objective: We present recurrent 15q11.2 (BP1-BP2) microdeletion encompassing NIPA1, NIPA2, CYFIP1, and TUBGCP5 in a family with phenotypic variability in developmental, speech, and motor delay. Case Report: A 32-year-old woman underwent amniocentesis
Externí odkaz:
https://doaj.org/article/745e3c62357b4651ace2028cbf8e7635