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sparse pubic syndrome相关文献:
Late-onset Rothmund-Thomson syndrome.
Kumar P, Sharma PK, Gautam RK, Jain RK, Kar HK.
Int J Dermatol. 2007 May;46(5):492-3. doi: 10.1111/j.1365-4632.2007.03248.x.
PMID:17472679
Androgen insensitivity.
Gottlieb B, Pinsky L, Beitel LK, Trifiro M.
Am J Med Genet. 1999 Dec 29;89(4):210-7. doi: 10.1002/(sici)1096-8628(19991229)89:4<210::aid-ajmg5>3.0.co;2-p.
PMID:10727996
Complete androgen insensitivity syndrome coexisting with mullerian duct remnants: a case report and literature review.
Chen DL, Guo S, Chen QL, Qiu SJ, Xu YY, Zhang J, Ma HM, Li YH.
Front Pediatr. 2024 Jun 4;12:1400319. doi: 10.3389/fped.2024.1400319. eCollection 2024.
PMID:38895190
A case of Kallmann syndrome.
Arkoncel ML, Arkoncel FR, Lantion-Ang FL.
BMJ Case Rep. 2011 Mar 25;2011:bcr0120113727. doi: 10.1136/bcr.01.2011.3727.
PMID:22700069
A rare disease of Kallmann syndrome: A case report.
Hilman S, Dewi DK, Kartika E.
Radiol Case Rep. 2023 Jan 12;18(3):1232-1238. doi: 10.1016/j.radcr.2022.12.036. eCollection 2023 Mar.
PMID:36660569
A Case of Primary Amenorrhea with Swyer Syndrome.
Priya PK, Mishra VV, Choudhary S, Rizvi JS.
J Hum Reprod Sci. 2017 Oct-Dec;10(4):310-312. doi: 10.4103/jhrs.JHRS_128_17.
PMID:29430160
Reproductive endocrine characteristics and in vitro fertilization treatment of female patients with partial 17α-hydroxylase deficiency: Two pedigree investigations and a literature review.
Jiang S, Xu Y, Qiao J, Wang Y, Kuang Y.
Front Endocrinol (Lausanne). 2022 Sep 14;13:970190. doi: 10.3389/fendo.2022.970190. eCollection 2022.
PMID:36187111
Primary seminoma of prostate in a patient with Klinefelter syndrome: A case report.
Shi D, Chen C, Huang H, Tian J, Zhou J, Jin S.
Medicine (Baltimore). 2022 Apr 29;101(17):e29117. doi: 10.1097/MD.0000000000029117.
PMID:35512069
Complete androgen insensitivity syndrome with a Sertoli-Leydig cell tumor.
Fagouri H, Moussaoui DR, Kouach J, Babahabib A, Oukabli M, Ameur A, Albouzidi A, Dehayni M.
J Pediatr Adolesc Gynecol. 2014 Oct;27(5):e113-5. doi: 10.1016/j.jpag.2013.08.007. Epub 2013 Dec 14.
PMID:24333107
Identification of the Rare Ala871Glu Mutation in the Androgen Receptor Gene Leading to Complete Androgen Insensitivity Syndrome in an Adolescent Girl with Primary Amenorrhea.
Kapama A, Papadimitriou DT, Mastorakos G, Vlahos NF, Papagianni M.
Children (Basel). 2022 Dec 3;9(12):1900. doi: 10.3390/children9121900.
PMID:36553343
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