LAMM Syndrome

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Tang, P. LAMM Syndrome. Encyclopedia. Available online: https://encyclopedia.pub/entry/6031 (accessed on 20 September 2026).

Tang P. LAMM Syndrome. Encyclopedia. Available at: https://encyclopedia.pub/entry/6031. Accessed September 20, 2026.

Tang, Peter. "LAMM Syndrome" Encyclopedia, https://encyclopedia.pub/entry/6031 (accessed September 20, 2026).

Tang, P. (2021, January 04). LAMM Syndrome. In Encyclopedia. https://encyclopedia.pub/entry/6031

Tang, Peter. "LAMM Syndrome." Encyclopedia. Web. 04 January, 2021.

LAMM Syndrome

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This entry is adapted from the peer-reviewed paper https://medlineplus.gov/genetics/condition/congenital-deafness-with-labyrinthine-aplasia-microtia-and-microdontia

Congenital deafness with labyrinthine aplasia, microtia, and microdontia (also called LAMM syndrome) is a condition that affects development of the ears and teeth.

genetic conditions

References

Alsmadi O, Meyer BF, Alkuraya F, Wakil S, Alkayal F, Al-Saud H, Ramzan K,Al-Sayed M. Syndromic congenital sensorineural deafness, microtia and microdontiaresulting from a novel homoallelic mutation in fibroblast growth factor 3 (FGF3).Eur J Hum Genet. 2009 Jan;17(1):14-21. doi: 10.1038/ejhg.2008.141.
Ordonez J, Tekin M. Congenital Deafness with Labyrinthine Aplasia, Microtia,and Microdontia. 2012 Sep 20 [updated 2019 Apr 4]. In: Adam MP, Ardinger HH,Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors. GeneReviews®[Internet]. Seattle (WA): University of Washington, Seattle; 1993-2020. Availablefrom http://www.ncbi.nlm.nih.gov/books/NBK100664/
Riazuddin S, Ahmed ZM, Hegde RS, Khan SN, Nasir I, Shaukat U, Riazuddin S,Butman JA, Griffith AJ, Friedman TB, Choi BY. Variable expressivity of FGF3mutations associated with deafness and LAMM syndrome. BMC Med Genet. 2011 Feb9;12:21. doi: 10.1186/1471-2350-12-21.
Tekin M, Hişmi BO, Fitoz S, Ozdağ H, Cengiz FB, Sirmaci A, Aslan I, InceoğluB, Yüksel-Konuk EB, Yilmaz ST, Yasun O, Akar N. Homozygous mutations infibroblast growth factor 3 are associated with a new form of syndromic deafnesscharacterized by inner ear agenesis, microtia, and microdontia. Am J Hum Genet.2007 Feb;80(2):338-44.
Tekin M, Oztürkmen Akay H, Fitoz S, Birnbaum S, Cengiz FB, Sennaroğlu L,Incesulu A, Yüksel Konuk EB, Hasanefendioğlu Bayrak A, Sentürk S, Cebeci I, UtineGE, Tunçbilek E, Nance WE, Duman D. Homozygous FGF3 mutations result incongenital deafness with inner ear agenesis, microtia, and microdontia. ClinGenet. 2008 Jun;73(6):554-65. doi: 10.1111/j.1399-0004.2008.01004.x.

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Subjects: Genetics & Heredity

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