143 related articles for article (PubMed ID: 38222995)
1. A Case Report of 17α-Hydroxylase Deficiency in Two Saudi Siblings With Different Karyotyping.
Elabd S; Almohareb O; AlJaroudi D; Al Zahrani A; Brema I
Cureus; 2024 Jan; 16(1):e52191. PubMed ID: 38222995
[TBL] [Abstract][Full Text] [Related]
2. Presentation, Diagnosis, and Follow-Up Characteristics of 17α-Hydroxylase Deficiency Cases with Exon 1-6 Deletion (Founder Mutation) in the CYP17A1Gene: 20-Year Single-Center Experience.
Dundar I; Akinci A; Camtosun E; Ciftci N; Kayas L
Sex Dev; 2023; 17(1):43-50. PubMed ID: 36652930
[TBL] [Abstract][Full Text] [Related]
3. A rare cause of delayed puberty and primary amenorrhea: 17α-hydroxylase enzyme deficiency.
Beştaş A; Bolu S; Unal E; Aktar Karakaya A; Eröz R; Tekin M; Haspolat YK
Endocrine; 2022 Mar; 75(3):927-933. PubMed ID: 34724156
[TBL] [Abstract][Full Text] [Related]
4. Clinical and Genetic Analyses of Two Unrelated 46, XX Girls with Combined 17α-Hydroxylase/17,20-lyase Deficiency from China.
Li Y; Han T; Wang Y; Gao J; Zhang J; Wu Y
J Clin Res Pediatr Endocrinol; 2023 Feb; ():. PubMed ID: 36800681
[TBL] [Abstract][Full Text] [Related]
5. A Rare Cause of Congenital Adrenal Hyperplasia: Clinical and Genetic Findings and Follow-up Characteristics of Six Patients with 17-Hydroxylase Deficiency Including Two Novel Mutations.
Kardelen AD; Toksoy G; Baş F; Yavaş Abalı Z; Gençay G; Poyrazoğlu Ş; Bundak R; Altunoğlu U; Avcı Ş; Najaflı A; Uyguner O; Karaman B; Başaran S; Darendeliler F
J Clin Res Pediatr Endocrinol; 2018 Jul; 10(3):206-215. PubMed ID: 29595516
[TBL] [Abstract][Full Text] [Related]
6. Genotypic Sex and Severity of the Disease Determine the Time of Clinical Presentation in Steroid 17α-Hydroxylase/17,20-Lyase Deficiency.
Kurnaz E; Kartal Baykan E; Türkyılmaz A; Yaralı O; Yavaş Abalı Z; Turan S; Bereket A; Çayır A; Guran T
Horm Res Paediatr; 2020; 93(9-10):558-566. PubMed ID: 33780934
[TBL] [Abstract][Full Text] [Related]
7. 17α-HYDROXYLASE/17, 20-LYASE DEFICIENCY: CLINICAL AND MOLECULAR CHARACTERIZATION OF EIGHT CHINESE PATIENTS.
Wu C; Fan S; Qian Y; Zhou Y; Jin J; Dai Z; Jiang L
Endocr Pract; 2017 May; 23(5):576-582. PubMed ID: 28225307
[TBL] [Abstract][Full Text] [Related]
8. Genetic diagnosis and clinical analysis of 17α-hydroxylase/17, 20-lyase deficiency combined with type 2 diabetes mellitus: A case report.
Zhang Y; Yuan Y
Medicine (Baltimore); 2023 Dec; 102(52):e36727. PubMed ID: 38206738
[TBL] [Abstract][Full Text] [Related]
9. A report of congenital adrenal hyperplasia due to 17α-hydroxylase deficiency in two 46,XX sisters.
Espinosa-Herrera F; Espín E; Tito-Álvarez AM; Beltrán LJ; Gómez-Correa D; Burgos G; Llamos A; Zurita C; Rojas S; Dueñas-Espín I; Cueva-Ludeña K; Salazar-Vega J; Pinto-Basto J
Gynecol Endocrinol; 2020 Jan; 36(1):24-29. PubMed ID: 31464148
[TBL] [Abstract][Full Text] [Related]
10. Congenital Adrenal Hyperplasia due to 17-alpha-hydoxylase/17,20-lyase Deficiency Presenting with Hypertension and Pseudohermaphroditism: First Case Report from Oman.
Mula-Abed WA; Pambinezhuth FB; Al-Kindi MK; Al-Busaidi NB; Al-Muslahi HN; Al-Lamki MA
Oman Med J; 2014 Jan; 29(1):55-9. PubMed ID: 24498484
[TBL] [Abstract][Full Text] [Related]
11. [Congenital adrenal hyperplasia].
Stanić M; Nesović M
Med Pregl; 1999; 52(11-12):447-54. PubMed ID: 10748766
[TBL] [Abstract][Full Text] [Related]
12. A late 17α-hydroxylase deficiency diagnosis that leads to the discovery of a new CYP17 gene mutation.
Guenego A; Morel Y; Ionesco O; Mallet D; Priou-Guesdon M
Ann Endocrinol (Paris); 2015 Feb; 76(1):71-4. PubMed ID: 25613935
[TBL] [Abstract][Full Text] [Related]
13. An elderly patient with 17α-hydroxylase deficiency misdiagnosed as primary aldosteronism: a case report.
Ishinoda Y; Uto A; Yamada Y; Okazaki M; Asada H; Wakamatsu S; Kurihara I; Shibata H; Ishii T; Hasegawa T; Kumagai H; Kasuga A
BMC Endocr Disord; 2022 Dec; 22(1):300. PubMed ID: 36461073
[TBL] [Abstract][Full Text] [Related]
14. A case of 17 alpha-hydroxylase deficiency.
Kim SM; Rhee JH
Clin Exp Reprod Med; 2015 Jun; 42(2):72-6. PubMed ID: 26161337
[TBL] [Abstract][Full Text] [Related]
15. A Rare Presentation of 17α Hydroxylase/17,20 Lyase Deficiency in a Patient with non-Hodgkin's Lymphoma: A Case Report.
Tekkeli N; Kurt I; Yalman N; Timur Ç; Demir Ş; Sağsak E
J Clin Res Pediatr Endocrinol; 2024 Jun; ():. PubMed ID: 38912718
[TBL] [Abstract][Full Text] [Related]
16. A rare cause of delayed puberty in two cases with 46,XX and 46,XY karyotype: 17 α-hydroxylase deficiency due to a novel variant in
Unal E; Yıldırım R; Taş FF; Tekin S; Ceylaner S; Haspolat YK
Gynecol Endocrinol; 2020 Aug; 36(8):739-742. PubMed ID: 31885295
[No Abstract] [Full Text] [Related]
17. Clinical Features of Unrecognized Congenital Adrenal Hyperplasia Due to 17α-hydroxylase Deficiency Since Adolescence: A Case Report.
Rashmi KG; Ravichandran L; Roy A; Naik D; Kamalanathan S; Sahoo J; Chapla A; Thomas N
J ASEAN Fed Endocr Soc; 2023; 38(2):131-134. PubMed ID: 38045661
[TBL] [Abstract][Full Text] [Related]
18. Two rare forms of congenital adrenal hyperplasia, 11β hydroxylase deficiency and 17-hydroxylase/17,20-lyase deficiency, presenting with novel mutations.
Bulsari K; Maple-Brown L; Falhammar H
Hormones (Athens); 2018 Mar; 17(1):127-132. PubMed ID: 29858860
[TBL] [Abstract][Full Text] [Related]
19. Identification of a homozygous c.1039C>T (p.R347C) variant in CYP17A1 in a 67-year-old female patient with partial 17α-hydroxylase/17,20-lyase deficiency.
Yamagata S; Kageyama K; Usui T; Saito K; Takayasu S; Usutani M; Terui K; Daimon M
Endocr J; 2022 Feb; 69(2):115-120. PubMed ID: 34483146
[TBL] [Abstract][Full Text] [Related]
20. Phenotypic Heterogeneity and Fertility Potential of Patients With 17-Hydroxylase/17,20-lyase Deficiency.
Xu Y; Jiang S; Yan Z; Niu Y; Du W; Liu B; Han B; Liu X; Zhao S; Song H; Kuang Y; Qiao J
J Clin Endocrinol Metab; 2022 May; 107(6):e2610-e2618. PubMed ID: 35043964
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
