U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

Congenital anomaly of tongue

MedGen UID:
510618
•Concept ID:
C0158662
•
Congenital Abnormality
Synonym: Congenital abnormality of tongue
SNOMED CT: Congenital anomaly of tongue (60447007); Congenital abnormality of tongue (60447007)

Professional guidelines

PubMed

Individualized treatment of congenital vascular malformations of the tongue.
Guntau M, Cucuruz B, Brill R, Bidakov O, Von der Heydt S, Deistung A, Wohlgemuth WA
Clin Hemorheol Microcirc 2023;83(4):421-429. doi: 10.3233/CH-221683. PMID: 36846994
Recognition, Evaluation, and Management of Pediatric Hereditary Angioedema.
Krack AT, Bernstein JA, Ruddy RM
Pediatr Emerg Care 2021 Apr 1;37(4):218-223. doi: 10.1097/PEC.0000000000002402. PMID: 33780405
Controversies in the diagnosis and management of the Robin sequence.
Mackay DR
J Craniofac Surg 2011 Mar;22(2):415-20. doi: 10.1097/SCS.0b013e3182074799. PMID: 21403570

Recent clinical studies

Therapy

Individualized treatment of congenital vascular malformations of the tongue.
Guntau M, Cucuruz B, Brill R, Bidakov O, Von der Heydt S, Deistung A, Wohlgemuth WA
Clin Hemorheol Microcirc 2023;83(4):421-429. doi: 10.3233/CH-221683. PMID: 36846994
Robin Sequence: Neonatal Mandibular Distraction.
Morrison KA, Collares MV, Flores RL
Clin Plast Surg 2021 Jul;48(3):363-373. Epub 2021 May 8 doi: 10.1016/j.cps.2021.03.005. PMID: 34051891
Ankyloglossia and Other Oral Ties.
Walsh J, McKenna Benoit M
Otolaryngol Clin North Am 2019 Oct;52(5):795-811. Epub 2019 Jul 25 doi: 10.1016/j.otc.2019.06.008. PMID: 31353141
Overgrowth Syndrome.
Li Y, Donnelly CG, Rivera RM
Vet Clin North Am Food Anim Pract 2019 Jul;35(2):265-276. doi: 10.1016/j.cvfa.2019.02.007. PMID: 31103180Free PMC Article
Orotracheal intubation.
Dauphinee K
Emerg Med Clin North Am 1988 Nov;6(4):699-713. PMID: 3056706

Prognosis

Skin and mucosal telangiectatic lesions in hereditary hemorrhagic telangiectasia patients.
Hyldahl SJ, El-Jaji MQ, Schuster A, Kjeldsen AD
Int J Dermatol 2022 Dec;61(12):1497-1505. Epub 2022 Jul 6 doi: 10.1111/ijd.16320. PMID: 35792874Free PMC Article
Down syndrome as a cause of abnormalities in the craniofacial region: A systematic literature review.
Kaczorowska N, Kaczorowski K, Laskowska J, Mikulewicz M
Adv Clin Exp Med 2019 Nov;28(11):1587-1592. doi: 10.17219/acem/112785. PMID: 31778604
The ontogeny of Robin sequence.
Logjes RJH, Breugem CC, Van Haaften G, Paes EC, Sperber GH, van den Boogaard MH, Farlie PG
Am J Med Genet A 2018 Jun;176(6):1349-1368. Epub 2018 Apr 25 doi: 10.1002/ajmg.a.38718. PMID: 29696787
Hanhart syndrome.
Dogan DG, Dogan M, Aslan M, Menekse E, Yakinci C
Genet Couns 2010;21(4):359-62. PMID: 21290964
Cancer in dyskeratosis congenita.
Alter BP, Giri N, Savage SA, Rosenberg PS
Blood 2009 Jun 25;113(26):6549-57. Epub 2009 Mar 12 doi: 10.1182/blood-2008-12-192880. PMID: 19282459Free PMC Article

Clinical prediction guides

Maternal folic acid supplementation and the risk of ankyloglossia (tongue-tie) in infants; a systematic review.
Rubin G, Stewart C, McGowan L, Woodside JV, Barrett G, Godfrey KM, Hall J
PLoS One 2023;18(11):e0294042. Epub 2023 Nov 3 doi: 10.1371/journal.pone.0294042. PMID: 37922258Free PMC Article
Xeroderma pigmentosum in Yemen.
Khatri ML
Int J Dermatol 2021 Mar;60(3):314-320. Epub 2021 Feb 4 doi: 10.1111/ijd.15395. PMID: 33538348
Overgrowth Syndrome.
Li Y, Donnelly CG, Rivera RM
Vet Clin North Am Food Anim Pract 2019 Jul;35(2):265-276. doi: 10.1016/j.cvfa.2019.02.007. PMID: 31103180Free PMC Article
Goldenhar syndrome: current perspectives.
Bogusiak K, Puch A, Arkuszewski P
World J Pediatr 2017 Oct;13(5):405-415. Epub 2017 Jun 15 doi: 10.1007/s12519-017-0048-z. PMID: 28623555
Hyper-IgE syndrome: dental implications.
Esposito L, Poletti L, Maspero C, Porro A, Pietrogrande MC, Pavesi P, Dellepiane RM, Farronato G
Oral Surg Oral Med Oral Pathol Oral Radiol 2012 Aug;114(2):147-53. doi: 10.1016/j.oooo.2012.04.005. PMID: 22769403

Recent systematic reviews

Maternal folic acid supplementation and the risk of ankyloglossia (tongue-tie) in infants; a systematic review.
Rubin G, Stewart C, McGowan L, Woodside JV, Barrett G, Godfrey KM, Hall J
PLoS One 2023;18(11):e0294042. Epub 2023 Nov 3 doi: 10.1371/journal.pone.0294042. PMID: 37922258Free PMC Article
Etiological diagnosis of macroglossia: Systematic review and diagnostic algorithm.
Dietrich E, Grimaux X, Martin L, Samimi M
Ann Dermatol Venereol 2022 Dec;149(4):228-237. Epub 2022 Oct 11 doi: 10.1016/j.annder.2022.03.011. PMID: 36229262
Down syndrome as a cause of abnormalities in the craniofacial region: A systematic literature review.
Kaczorowska N, Kaczorowski K, Laskowska J, Mikulewicz M
Adv Clin Exp Med 2019 Nov;28(11):1587-1592. doi: 10.17219/acem/112785. PMID: 31778604
Craniofacial and upper airway morphology in adult obstructive sleep apnea patients: A systematic review and meta-analysis of cephalometric studies.
Neelapu BC, Kharbanda OP, Sardana HK, Balachandran R, Sardana V, Kapoor P, Gupta A, Vasamsetti S
Sleep Med Rev 2017 Feb;31:79-90. Epub 2016 Jan 30 doi: 10.1016/j.smrv.2016.01.007. PMID: 27039222
Treatment of ankyloglossia and breastfeeding outcomes: a systematic review.
Francis DO, Krishnaswami S, McPheeters M
Pediatrics 2015 Jun;135(6):e1458-66. Epub 2015 May 4 doi: 10.1542/peds.2015-0658. PMID: 25941303Free PMC Article

Supplemental Content

Table of contents

    Practice guidelines

    • PubMed
      See practice and clinical guidelines in PubMed. The search results may include broader topics and may not capture all published guidelines. See the FAQ for details.
    • Bookshelf
      See practice and clinical guidelines in NCBI Bookshelf. The search results may include broader topics and may not capture all published guidelines. See the FAQ for details.

    Related information

    • PMC Articles
      Related information in PubMed Central Links
    • PubMed
      Related literature resources in PubMed

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...