Your browser does not fully support modern features. Please upgrade for a smoother experience.
Submitted Successfully!
Thank you for your contribution! You can also upload a video entry or images related to this topic. For video creation, please contact our Academic Video Service.
Version Summary Created by Modification Content Size Created at Operation
1 Camila Xu + 659 word(s) 659 2020-12-15 07:29:48

Video Upload Options

We provide professional Academic Video Service to translate complex research into visually appealing presentations. Would you like to try it?
No, upload directly Yes
Cite
If you have any further questions, please contact Encyclopedia Editorial Office.
Xu, C. Leydig Cell Hypoplasia. Encyclopedia. Available online: https://encyclopedia.pub/entry/4573 (accessed on 29 September 2026).
Xu C. Leydig Cell Hypoplasia. Encyclopedia. Available at: https://encyclopedia.pub/entry/4573. Accessed September 29, 2026.
Xu, Camila. "Leydig Cell Hypoplasia" Encyclopedia, https://encyclopedia.pub/entry/4573 (accessed September 29, 2026).
Xu, C. (2020, December 24). Leydig Cell Hypoplasia. In Encyclopedia. https://encyclopedia.pub/entry/4573
Xu, Camila. "Leydig Cell Hypoplasia." Encyclopedia. Web. 24 December, 2020.
Leydig Cell Hypoplasia
Edit
This entry is adapted from the peer-reviewed paper https://medlineplus.gov/genetics/condition/leydig-cell-hypoplasia

Leydig cell hypoplasia is a condition that affects male sexual development. It is characterized by underdevelopment (hypoplasia) of Leydig cells in the testes. Leydig cells secrete male sex hormones (androgens) that are important for normal male sexual development before birth and during puberty.

genetic conditions

References

  1. Kossack N, Simoni M, Richter-Unruh A, Themmen AP, Gromoll J. Mutations in anovel, cryptic exon of the luteinizing hormone/chorionic gonadotropin receptorgene cause male pseudohermaphroditism. PLoS Med. 2008 Apr 22;5(4):e88. doi:10.1371/journal.pmed.0050088.
  2. Qiao J, Han B, Liu BL, Chen X, Ru Y, Cheng KX, Chen FG, Zhao SX, Liang J, LuYL, Tang JF, Wu YX, Wu WL, Chen JL, Chen MD, Song HD. A splice site mutationcombined with a novel missense mutation of LHCGR cause malepseudohermaphroditism. Hum Mutat. 2009 Sep;30(9):E855-65. doi:10.1002/humu.21072.
  3. Themmen AP, Verhoef-Post M. LH receptor defects. Semin Reprod Med. 2002Aug;20(3):199-204. Review.
  4. Wu SM, Chan WY. Male pseudohermaphroditism due to inactivating luteinizinghormone receptor mutations. Arch Med Res. 1999 Nov-Dec;30(6):495-500. Review.
  5. Wu SM, Leschek EW, Rennert OM, Chan WY. Luteinizing hormone receptor mutationsin disorders of sexual development and cancer. Front Biosci. 2000 Mar1;5:D343-52. Review.
More
©Text is available under the terms and conditions of the Creative Commons-Attribution ShareAlike (CC BY-SA) license; additional terms may apply. By using this site, you agree to the Terms and Conditions and Privacy Policy.
Upload a video for this entry
Information
Subjects: Genetics & Heredity
Contributor MDPI registered users' name will be linked to their SciProfiles pages. To register with us, please refer to https://encyclopedia.pub/register : Camila Xu
View Times: 707
Entry Collection: MedlinePlus
Revision: 1 time (View History)
Update Date: 24 Dec 2020
Table of Contents
    Notice
    You are not a member of the advisory board for this topic. If you want to update advisory board member profile, please contact office@encyclopedia.pub.
    OK
    Confirm
    Only members of the Encyclopedia advisory board for this topic are allowed to note entries. Would you like to become an advisory board member of the Encyclopedia?
    Yes
    No
    ${ textCharacter }/${ maxCharacter }
    Submit
    Cancel
    There is no comment~
    ${ textCharacter }/${ maxCharacter }
    Submit
    Cancel
    ${ selectedItem.replyTextCharacter }/${ selectedItem.replyMaxCharacter }
    Submit
    Cancel
    Confirm
    Are you sure to Delete?
    Yes No
    Academic Video Service
    Feedback