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 + 467 word(s) 467 2020-12-15 07:30:01

Video Upload Options

We provide professional Academic Video Service to translate complex research into visually appealing presentations. Would you like to try it?
Cite
If you have any further questions, please contact Encyclopedia Editorial Office.
Xu, C. Lujan Syndrome. Encyclopedia. Available online: https://encyclopedia.pub/entry/4563 (accessed on 25 September 2026).
Xu C. Lujan Syndrome. Encyclopedia. Available at: https://encyclopedia.pub/entry/4563. Accessed September 25, 2026.
Xu, Camila. "Lujan Syndrome" Encyclopedia, https://encyclopedia.pub/entry/4563 (accessed September 25, 2026).
Xu, C. (2020, December 24). Lujan Syndrome. In Encyclopedia. https://encyclopedia.pub/entry/4563
Xu, Camila. "Lujan Syndrome." Encyclopedia. Web. 24 December, 2020.
Lujan Syndrome
Edit

Lujan syndrome is a condition characterized by intellectual disability, behavioral problems, and certain physical features. It occurs almost exclusively in males.

genetic conditions

References

  1. Lerma-Carrillo I, Molina JD, Cuevas-Duran T, Julve-Correcher C,Espejo-Saavedra JM, Andrade-Rosa C, Lopez-Muñoz F. Psychopathology in theLujan-Fryns syndrome: report of two patients and review. Am J Med Genet A. 2006Dec 15;140(24):2807-11. Review.
  2. Lujan JE, Carlin ME, Lubs HA. A form of X-linked mental retardation withmarfanoid habitus. Am J Med Genet. 1984 Jan;17(1):311-22.
  3. Lyons MJ. MED12-Related Disorders. 2008 Jun 23 [updated 2016 Aug 11]. In: AdamMP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle;1993-2020. Available from http://www.ncbi.nlm.nih.gov/books/NBK1676/
  4. Schwartz CE, Tarpey PS, Lubs HA, Verloes A, May MM, Risheg H, Friez MJ,Futreal PA, Edkins S, Teague J, Briault S, Skinner C, Bauer-Carlin A, SimensenRJ, Joseph SM, Jones JR, Gecz J, Stratton MR, Raymond FL, Stevenson RE. Theoriginal Lujan syndrome family has a novel missense mutation (p.N1007S) in theMED12 gene. J Med Genet. 2007 Jul;44(7):472-7.
  5. Van Buggenhout G, Fryns JP. Lujan-Fryns syndrome (mental retardation,X-linked, marfanoid habitus). Orphanet J Rare Dis. 2006 Jul 10;1:26. Review.
More
Upload a video for this entry
Information
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: 1.2K
Entry Collection: MedlinePlus
Revision: 1 time (View History)
Update Date: 24 Dec 2020
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