Relevant bibliographies by topics / Aglossia

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters

Academic literature on the topic 'Aglossia'

Author: Grafiati
Published: 4 June 2021
Last updated: 1 February 2022

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Journal articles on the topic "Aglossia"

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McMicken, Betty, Margaret Vento-Wilson, Mary Warden, Melissa Hall, and Kelly Rogers. "A Child With Congenital Aglossia: A Narrative Review and Descriptive Case Study." SAGE Open 9, no. 1 (January 2019): 215824401882451. http://dx.doi.org/10.1177/2158244018824515.

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This article details an account of a young female with congenial aglossia. Because of the low incidence of this anatomical and physiological presentation, this narrative review includes a brief historical review of the disorder and a detailed description of: (1) reports in the literature of congenital hypoglossia and aglossia, (2) characteristics of speech in children with congenital aglossia below the age of 18 years, and (3) the medical history, speech acquisition, and course of intervention of a 5-year-old girl with congenital aglossia currently in speech treatment.
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Elnaggar, Alaa, and Noha A. Azab. "A case of isolated aglossia." Journal of Oral Medicine and Oral Surgery 24, no. 3 (October 2018): 149–50. http://dx.doi.org/10.1051/mbcb/2018014.

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Introduction: Aglossia is a rare condition of failure of development of the lateral lingual swellings during embryogenesis and is usually associated with other deformities especially the fingers and limbs. Isolated aglossia is extremely rare. Observation: This is a case report of a 21-year-old patient with isolated aglossia whose floor of the mouth compensated for the tongue's absence in speech, eating and swallowing. Thus the patient did not express any disability and refused reconstructive treatment. Commentaries: Aglossia may be accompanied by many deformities or as part of a syndrome, so other symptoms must be excluded. The floor of the mouth usually adapts to the role of the tongue leading to fulfillment of most of the functions of the tongue. Conclusion: Aglossia is a rare condition, however the adaptation of the surrounding tissues compensated for the absence of the tongue makes the condition tolerable to the patient, this however does not undermine the fact that a multidisciplinary approach is key in managing such a condition.
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Kugushev, Alexander Yu, A. V. Lopatin, and S. A. Yasonov. "HYPOGLOSSIA: LITERATURE REVIEW AND TWO CASES." Russian Journal of Pediatric Surgery 23, no. 4 (September 17, 2019): 206–10. http://dx.doi.org/10.18821/1560-9510-2019-23-4-206-210.

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Introduction. Aglossia / hypoglossia is a rare condition combined with underdeveled lower jaw, lack of mandibular incisors and various degrees of limb anomalies. In domestic and foreign literature, one can find only few such observations in pediatric and adult populations. This malformation is met in the syndrome of limb and oromandibular hypogynesia or aglossia-adactylia syndrome. The incidence of aglossia / hypoglossia is very low (1 / 175,000-1 / 1,000,000 live births, ) and in most cases it is represented by hypoglosia, and not true aglossia. The isolated aglossia without limb malformations is an even more rare condition. The etiology of aglossia / hypoglosia is unknown, since all known cases are sporadic and by present moment no more than 100 observations have been published. Material and methods. In 2015, a girl (1 year 10 mon old ) and a 3- year old boy were examined in hospital and outpatiently because of complaints for the reduction of lower jaw. The children were examined by an orthodontist; additional examinations were prescribed to the girl because of revealed comorbidities. Results. The girl also had vertebrae malformation. Such a pathological combination had not been seen previously in the available literature. The second child was a boy of 3 y.o.; his parents decided to consult an orthodontist for correcting the bite. In both cases, children were well adapted, although there were some deficiencies in verbal activity and difficulties in feeding; after speech therapy and spoon-feeding trainings these problems were solved. Conclusion. Even with a significant degree of tongue underdevelopment, there are practically no functional limitations in patients with aglossia-adactyl syndrome, which is important for determining prognosis as well as for consulting patients and their parents and for making decision about the need for corrective surgery.
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Bommarito, Silvana, Luciana Zanato, Marilena Vieira, and Fernanda Angelieri. "Aglossia: Case Report." International Archives of Otorhinolaryngology 20, no. 01 (January 30, 2015): 087–92. http://dx.doi.org/10.1055/s-0034-1544116.

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Introduction Aglossia is a rare condition caused by failure of the tongue embryogenesis process (in the fourth to eighth weeks of gestation). The tongue is an organ used in different activities such as sucking, swallowing, chewing, and talking. It is also responsible for shaping palate dental arches (in its absence, they become atrophic). There are few similar cases reported in the literature. Objective To describe a rare case of aglossia and the multidisciplinary professionals working together for 5 years to treat the patient. Resumed Report An 8-year-old girl with aglossia had an assessment comprising: (1) clinical assessment of the stomatognathic system related to resting posture, tonus, and mobility; (2) orthodontic assessment; (3) surface electromyography of the chewing muscles; (4) swallowing videofluoroscopy. Conclusion The authors confirmed the need of multidisciplinary cooperation to improve the patient's quality of life, because agenesia implicates many activities/functions that depend on the tongue to fully work. Multiprofessional cooperation helps the patient learn compensation mechanisms.
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Higashi, Koichiro, and Masataka Edo. "Conductive deafness in aglossia." Journal of Laryngology & Otology 110, no. 11 (November 1996): 1057–59. http://dx.doi.org/10.1017/s0022215100135741.

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AbstractAglossia is a rare anomaly often accompanied with several congenital defects including varying degrees of limb deficiency, micrognathia and oral synechiae. We report on a girl with aglossia and persistent anterior buccopharyngeal membrane. Other anomalies observed on the patient were oesophageal atresia, hypoplastic epiglottis, ptosis of the left eyelid, and conductive deafness which is probably an additional symptom of this syndrome group.
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Kumar, Prashant, and KK Chaubey. "Aglossia: A case report." Journal of Indian Society of Pedodontics and Preventive Dentistry 25, no. 1 (2007): 46. http://dx.doi.org/10.4103/0970-4388.31991.

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7

Dunham, Michael E., and Thomas L. Austin. "Congenital aglossia and situs inversus." International Journal of Pediatric Otorhinolaryngology 19, no. 2 (June 1990): 163–68. http://dx.doi.org/10.1016/0165-5876(90)90222-d.

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8

YOKOE, Yoshihiko, Yukitada HYO, Yasuhiro HIROOKA, Tadahiko IIZUKA, and Takatoki ONO. "A case of the congenital aglossia." Japanese Journal of Oral & Maxillofacial Surgery 31, no. 10 (1985): 2450–56. http://dx.doi.org/10.5794/jjoms.31.2450.

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Purohit, Shrirang K., Samir M. Kumta, Posani Pardhasarathy Rao, and Ravin L. Thatte. "An interesting case of aglossia-adactyly syndrome." British Journal of Plastic Surgery 42, no. 2 (March 1989): 228–29. http://dx.doi.org/10.1016/0007-1226(89)90209-9.

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Kantaputra, Piranit, and Pranoot Tanpaiboon. "Thyroid dysfunction in a patient with aglossia." American Journal of Medical Genetics 122A, no. 3 (September 4, 2003): 274–77. http://dx.doi.org/10.1002/ajmg.a.20269.

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Dissertations / Theses on the topic "Aglossia"

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Valent, Franziska G. "Taste testing in a pediatric case of congenital aglossia." Thesis, California State University, Long Beach, 2016. http://pqdtopen.proquest.com/#viewpdf?dispub=10195967.

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Congenital aglossia (CA) is a very rare condition in which a person is born without a tongue. This current study sought to investigate the taste function of an 11-year-old female with CA. In this randomized, double-blinded, controlled taste test trial, the participant was asked to identify different concentration levels of sweet, sour, salty, bitter, and umami tastant solutions. Responses were analyzed for correct identification. Out of the five stimuli, the participant correctly identified sour at 1.6 x 10-4 M and umami at 5.0 x 10-3 M. Sweet, salty, and bitter stimuli did not meet the accuracy identification threshold of 66.6% at any concentration level. Statistical significant association between taste identification accuracy and actual taste [X²(5) = 7.674, p = .175], individual stimuli concentration levels (sweet p = .645; sour p = .558; salty p = .484; umami p = .061), and presentation order [X²(5) = 55.000, p = .437] could not be determined using Chi-square testing. Findings suggest an alteration in taste function in individuals with CA.

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Millington, Grethel. "Primary Cilia-dependent Gli Processing in Neural Crest Cells is Required for Early Tongue Development." University of Cincinnati / OhioLINK, 2016. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1479815997983138.

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Books on the topic "Aglossia"

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Nieden. Amphibia. Anura I.: Subordo Aglossa und Phaneroglossa, Sectio I Arcifera. De Gruyter, Inc., 2020.

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Book chapters on the topic "Aglossia"

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"Hypoglossia/Aglossia (Hanhart syndrome)." In Encyclopedia of Genetics, Genomics, Proteomics and Informatics, 946. Dordrecht: Springer Netherlands, 2008. http://dx.doi.org/10.1007/978-1-4020-6754-9_8110.

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