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Journal articles on the topic 'Aglossia'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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1

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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2

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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3

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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4

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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5

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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6

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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9

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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10

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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11

Isono, Shinsaku, Yasushi Ohashi, Akihiko Iida, and Michi Nishikiori. "Assessment of Articulation of Child with Congenital Aglossia." Japan Journal of Logopedics and Phoniatrics 34, no. 2 (1993): 149–57. http://dx.doi.org/10.5112/jjlp.34.149.

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12

Simpson, Adrian P., and Gottfried Meinhold. "Compensatory articulations in a case of congenital aglossia." Clinical Linguistics & Phonetics 21, no. 7 (January 2007): 543–56. http://dx.doi.org/10.1080/02699200701368787.

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13

Jang, G. Y., K. C. Lee, J. T. Choung, C. S. Son, and Y. C. Tockgo. "Congenital aglossia with situs inversus totalis--a case report." Journal of Korean Medical Science 12, no. 1 (1997): 55. http://dx.doi.org/10.3346/jkms.1997.12.1.55.

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14

Tuncbilek, Ergul, Cengiz Yalcin, and Metin Atasu. "Aglossia-adactylia syndrome (special emphasis on the inheritance pattern)." Clinical Genetics 11, no. 5 (April 23, 2008): 421–23. http://dx.doi.org/10.1111/j.1399-0004.1977.tb01338.x.

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15

Hegazy, Mohamed, Hesham Farag, and Mohamed Naguib. "Anesthetic Management of Aglossia-Adactylia Syndrome: Report of a Case." Annals of Saudi Medicine 8, no. 3 (May 1988): 221–23. http://dx.doi.org/10.5144/0256-4947.1988.221.

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16

Sumitomo, Asako, Hirokazu Sakamoto, Hiroaki Hatano, Yoshiyuki Tanaka, and Masahide Otsu. "The Course of Language Acquisition in an Infant with Aglossia." Japan Journal of Logopedics and Phoniatrics 59, no. 3 (2018): 251–59. http://dx.doi.org/10.5112/jjlp.59.251.

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17

WALKER, PJ, MJ EDWARDS, V. PETROFF, I. WILSON, AD TEMPERLEY, and J. SEABROOK. "Agnathia (severe microghathia), aglossia and choanal atresia in an infant." Journal of Paediatrics and Child Health 31, no. 4 (August 1995): 358–61. http://dx.doi.org/10.1111/j.1440-1754.1995.tb00828.x.

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18

Clouthier, David E., Marthe Howard, and Francie Hyndman. "Hand2 loss leads to aglossia from failure to repress Dlx5/6." Developmental Biology 331, no. 2 (July 2009): 526. http://dx.doi.org/10.1016/j.ydbio.2009.05.519.

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19

McMicken, Betty L., Andrew Kunihiro, Long Wang, Frederico Salles, Patrícia Costa Bezerra, and Kelly Rogers. "Randomized testing of taste discrimination in a case of congenital aglossia." Journal of Oral Biology and Craniofacial Research 4, no. 2 (May 2014): 120–26. http://dx.doi.org/10.1016/j.jobcr.2014.08.001.

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20

Yuan, Gongjie, Gurpreet Singh, Serafine Chen, Kristy Carrington Perez, Yan Wu, Bo Liu, and Jill Ann Helms. "Cleft Palate and Aglossia Result from Perturbations in Wnt and Hedgehog Signaling." Cleft Palate-Craniofacial Journal 54, no. 3 (May 2017): 269–80. http://dx.doi.org/10.1597/15-178.

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Objective The objective of this study was to explore the molecular basis for cleft secondary palate and arrested tongue development caused by the loss of the intraflagellar transport protein, Kif3a. Design Kif3a mutant embryos and their littermate controls were analyzed for defects in facial development at multiple stages of embryonic development. Histology was employed to understand the effects of Kif3a deletion on palate and tongue development. Various transgenic reporter strains were used to understand how deletion of Kif3a affected Hedgehog and Wnt signaling. Immunostaining for structural elements of the tongue and for components of the Wnt pathway were performed. BrdU activity analyses were carried out to examine how the loss of Kif3a affected cell proliferation and led to palate and tongue malformations. Results Kif3a deletion causes cranial neural crest cells to become unresponsive to Hedgehog signals and hyper-responsive to Wnt signals. This aberrant molecular signaling causes abnormally high cell proliferation, but paradoxically outgrowths of the tongue and the palatal processes are reduced. The basis for this enigmatic effect can be traced back to a disruption in epithelial/mesenchymal signaling that governs facial development. Conclusion The primary cilium is a cell surface organelle that integrates Hh and Wnt signaling, and disruptions in the function of the primary cilium cause one of the most common—of the rarest—craniofacial birth defects observed in humans. The shared molecular basis for these dysmorphologies is an abnormally high Wnt signal simultaneous with an abnormally low Hedgehog signal. These pathways are integrated in the primary cilium.

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21

Hyndman, Francie E., Marthe Howard, and David E. Clouthier. "Aglossia in Hand2 conditional knockout mutants results from misregulation of Dlx5/6." Developmental Biology 344, no. 1 (August 2010): 443–44. http://dx.doi.org/10.1016/j.ydbio.2010.05.129.

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22

McMicken, Betty, Shelley Von Berg, and Khalil Iskarous. "Acoustic and Perceptual Description of Vowels in a Speaker With Congenital Aglossia." Communication Disorders Quarterly 34, no. 1 (March 19, 2012): 38–46. http://dx.doi.org/10.1177/1525740111435114.

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The goals of this study were to (a) compare the vowel space produced by a person with congenital aglossia (PWCA) with a typical vowel space; (b) investigate listeners’ intelligibility for single vowels produced by the PWCA, with and without visual information; and (c) determine whether there is a correlation between scores of speech intelligibility of PWCA speech and the acoustic properties of those speech samples. The main objective of this study was to determine whether a PWCA was able to compensate for the lack of tongue and whether listeners were able to compensate perceptually for the possible atypical acoustics of the PWCA. Cineradiography for this article was limited to observation of gross function of the tongue base and mylohyoid. An audiovisual recording of the PWCA speaker’s output was obtained for a series of isolated vowels, diphthongized vowels, and vowels in monosyllables. Production of vowels was analyzed acoustically and perceptually. Vowels were presented to listeners under two conditions: audiovisual and audio only. Paired differences sample tests revealed no statistical differences in intelligibility for the audio versus audiovisual conditions. Mean intelligibility for vowels was 78.5% overall. Intelligibility was a function of vowel position, with the front vowels revealing the least intelligibility and the back vowels revealing the greatest intelligibility. Quantitative analysis of F1–F2 formant data revealed that the speaker’s front vowels showed greater distances from the back vowels when compared with the F1–F2 means of normative data.

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23

McMicken, Betty, Margaret Vento-Wilson, Shelley Von Berg, Khalil Iskarous, Namhee Kim, Kelly Rogers, and Sonja Young. "Semantic and Phonemic Listener Confusions in a Case of Isolated Congenital Aglossia." Communication Disorders Quarterly 35, no. 2 (October 2013): 74–83. http://dx.doi.org/10.1177/1525740113504383.

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24

Grippaudo, Francesca Romana, and Daniel Christopher Kennedy. "Oromandibular-limb hypogenesis syndromes: a case of aglossia with an intraoral band." British Journal of Plastic Surgery 51, no. 6 (September 1998): 480–83. http://dx.doi.org/10.1054/bjps.1997.0207.

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25

Neidich, Julie A., Linton A. Whitaker, Marvin Natowicz, Donna M. McDonald, Rhonda Schnur, Elaine H. Zackai, John M. Opitz, James F. Reynolds, and Robert J. Gorlin. "Aglossia with congenital absence of the mandibular rami and other craniofacial abnormalities." American Journal of Medical Genetics 31, S4 (1988): 161–66. http://dx.doi.org/10.1002/ajmg.1320310516.

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26

Faqeih, Eissa, Hassan Farra, and Zuhair Al-Hassnan. "A further case of micrognathia, aglossia, and situs inversus totalis with additional features." Clinical Dysmorphology 17, no. 3 (July 2008): 219–20. http://dx.doi.org/10.1097/mcd.0b013e3282f73731.

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27

McMicken, Betty, Margaret Vento-Wilson, Shelley Von Berg, and Kelly Rogers. "Cineradiographic Examination of Articulatory Movement of Pseudo-Tongue, Hyoid, and Mandible in Congenital Aglossia." Communication Disorders Quarterly 36, no. 1 (March 18, 2014): 3–11. http://dx.doi.org/10.1177/1525740114523310.

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This research examined cineradiographic films (CRF) of articulatory movements in a person with congenital aglossia (PWCA) during speech production of four phrases. Pearson correlations and a multiple regression model investigated co-variation of independent variables, positions of mandible and hyoid; and pseudo-tongue-dependent variables, positions of mylohyoid and tongue base. Results suggest that backing/fronting of the mandible assisted the mylohyoid/tongue base in making mid-antero-posterior constrictions. Co-linearity findings suggest the best predictor of tongue base movement was mandible for back sounds. Hyoid movement was highly correlated with mandibular movement horizontally, but hyoid acted independently vertically and possibly with greater phonemic specialty in the PWCA. Findings suggest hyoid was a strong determinant of vertically dependent variable movement in all phrases. The extent of hyoid activity was a unique finding and one that may begin to explain relative intelligibility in this PWCA. Observed changes in vocal tract length may have influenced F2 transitional/vowel midpoint values.

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28

Gupta, ShaliniR. "Isolated aglossia congenita: A rare case of oromandibular limb hypogenesis syndrome type I B." Journal of Oral and Maxillofacial Pathology 16, no. 3 (2012): 414. http://dx.doi.org/10.4103/0973-029x.102504.

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29

Ren, X. C., Y. F. Li, Y. Liu, and S. S. Zhu. "Mandibular symphyseal midline distraction osteogenesis for micrognathia associated with aglossia and situs inversus totalis." International Journal of Oral and Maxillofacial Surgery 46, no. 10 (October 2017): 1346–51. http://dx.doi.org/10.1016/j.ijom.2017.05.019.

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30

Salles, Frederico, Marcos Anchieta, Patrícia Costa Bezerra, Maria Lúcia G. M. Torres, Elizabeth Queiroz, and Jorge Faber. "Complete and isolated congenital aglossia: case report and treatment of sequelae using rapid prototyping models." Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontology 105, no. 3 (March 2008): e41-e47. http://dx.doi.org/10.1016/j.tripleo.2007.09.028.

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31

Rasool, Altaf, Mohammad Inam Zaroo, Adil Hafeez Wani, Mohammad Ashraf Darzi, Shiekh Adil Bashir, Akram Hussain Bijli, and Shafaq Rashid. "Isolated aglossia in a six year old child presenting with impaired speech: a case report." Cases Journal 2, no. 1 (2009): 7926. http://dx.doi.org/10.4076/1757-1626-2-7926.

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32

Ramírez-Cheyne, Julián, Harry Pachajoa, Carolina Isaza, and Wilmar Saldarriaga. "Síndrome de aglosia-adactilia y exposición prenatal a misoprostol ¿Relación causal o casual? Reporte de un caso." Revista Colombiana de Obstetricia y Ginecología 59, no. 3 (September 30, 2008): 248–52. http://dx.doi.org/10.18597/rcog.411.

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Introducción y objetivo: el síndrome de aglosia-adactilia es un síndrome polimalformativo congénito de muy baja frecuencia, con una etiología y patrón de herencia que no son claros. Se hace una búsqueda bibliográfica orientada a la asociación entre la exposición prenatal a misoprostol y malformaciones congénitas. Se presenta un caso de este síndrome asociado a exposición prenatal a misoprostol a las 10 semanas de gestación, asociación no establecida en la literatura revisada.Presentación del caso: recién nacido con características fenotípicas de síndrome de aglosia-adactilia, hijo de madre de 17 años, con antecedente de haber utilizado misoprostol en dosis de 400 microgramos vía oral y 200 microgramos vía vaginal a las 10 semanas de gestación, con el objetivo de interrumpir el embarazo.Discusión: el misoprostol es un análogo sintético de la prostaglandina E1, se ha asociado a un aumento en el riesgo de la ocurrencia de secuencia de Moebius, artrogriposis, síndrome de aglosia-adactilia, defectos de las extremidades de tipo terminal y transversal en madres que utilizan este medicamento durante el primer trimestre de gestación.

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33

Toutios, Asterios, Dani Byrd, Louis Goldstein, and Shrikanth S. Narayanan. "Articulatory compensation strategies employed by an aglossic speaker." Journal of the Acoustical Society of America 142, no. 4 (October 2017): 2639. http://dx.doi.org/10.1121/1.5014671.

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34

Hu, Zhong-Wen, Li-Kun Zhong, Chang Han, Hong-Li He, Jian-Feng Liu, and Mao-Fa Yang. "The complete mitochondrial genome sequence of Aglossa dimidiata (Haworth, 1809) (Lepidoptera: Pyralidae)." Mitochondrial DNA Part B 6, no. 10 (September 17, 2021): 2967–68. http://dx.doi.org/10.1080/23802359.2021.1974965.

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35

Sánchez Piñero, F., and F. J. Pérez López. "Coprophagy in Lepidoptera: observational and experimental evidence in the pyralid moth Aglossa pinguinalis." Journal of Zoology 244, no. 3 (March 1998): 357–62. http://dx.doi.org/10.1017/s0952836998003069.

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36

Sanchez Pinero, F., and F. J. Perez Lopez. "Coprophagy in Lepidoptera: observational and experimental evidence in the pyralid moth Aglossa pinguinalis." Journal of Zoology 244, no. 3 (March 1998): 357–62. http://dx.doi.org/10.1111/j.1469-7998.1998.tb00040.x.

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37

Procter, Joan B. "On the Variation of the Scapula in the Batrachian Groups Aglossa and Arcifera." Proceedings of the Zoological Society of London 91, no. 2 (August 21, 2009): 197–214. http://dx.doi.org/10.1111/j.1096-3642.1921.tb03259.x.

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38

Toutios, Asterios, Melissa Xu, Dani Byrd, Louis Goldstein, and Shrikanth Narayanan. "How an aglossic speaker produces an alveolar-like percept without a functional tongue tip." Journal of the Acoustical Society of America 147, no. 6 (June 2020): EL460—EL464. http://dx.doi.org/10.1121/10.0001329.

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39

Grehan, JR. "A panbiogeographic perspective for pre-cretaceous angiosperm–Lepidoptera coevolution." Australian Systematic Botany 4, no. 1 (1991): 91. http://dx.doi.org/10.1071/sb9910091.

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The coevolutionary history of Lepidoptera and angiosperms is evaluated in relation to Croizat's panbiogeographic synthesis of angiosperm evolution. The panbiogeographic method of ocean basin classification is used to identify major patterns of trans-oceanic distribution for lepidopteran families and genera (principally non-ditrysian). The Pacific basin is identified as a major evolutionary centre for several 'primitive non-ditrysian Lepidoptera, including Zeugloptera, Aglossata, Heterobathmiina, Neopsuestina, Palaephatidae, Prodoxidae, and possibly the Dacnonypha. The ditrysian Ithomiidae are similarly classified with the Pacific while the related Daniidae are identified as Indian Ocean. An Indian Ocean baseline is proposed for the Callidulidae, Tinissimae and Perissomasticini (Tineidae). A 'coevolutionary' history is supported in terms of Lepidoptera and angiosperms sharing common biogeographic (spatiotemporal) characters associated with the pre-Cretaceous tectonic history of major ocean and sea basins. The lack of congruent higher level Lepidoptera-angiosperm phylogenies emerging from systematic studies may be due to a lack of cospeciation events, but this does not exclude a close ecological and evolutionary relationship through the history of both groups.

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40

L McMicken, Betty. "Electropalatography in a Case of Congenital Aglossia." Journal of Communication Disorders, Deaf Studies & Hearing Aids 02, no. 03 (2014). http://dx.doi.org/10.4172/2375-4427.1000113.

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41

Kaissi, A., H. Safi, MB Ghachem, L. Hendaoui, and F. Chehida. "Aglossia-adactylia sequence and Moebius syndrome involvement." African Journal of Oral Health 2, no. 1-2 (July 26, 2010). http://dx.doi.org/10.4314/ajoh.v2i1-2.57005.

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42

Valent, Franziska, Long Wang, Betty McMicken, Cheryl Rock, and Vivianna Goh. "Taste Testing in a Pediatric Case of Congenital Aglossia." Journal of Communication Disorders, Deaf Studies & Hearing Aids 05, no. 03 (2017). http://dx.doi.org/10.4172/2375-4427.1000179.

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McMicken, Betty L. "Speech and Swallow Kinematics of a Person with Congenital Aglossia." Anatomy & Physiology 05, no. 02 (2015). http://dx.doi.org/10.4172/2161-0940.1000174.

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McMicken, Betty L., Shelley Von Berg, and Long Wang Andrew Kunihiro. "Speech and Swallow Kinematics of a Person with Congenital Aglossia." Anatomy & Physiology 05, no. 03 (2015). http://dx.doi.org/10.4172/2161-0940.1000176.

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45

McMicken, Betty, Frederico Salles, Shelley Von Berg, Margaret Vento Wilson, Kelly Rogers, Asterios Toutios, and Shrikanth S. Narayanan. "Bilabial Substitution Patterns during Consonant Production in a Case of Congenital Aglossia." Journal of Communication Disorders, Deaf Studies & Hearing Aids 05, no. 02 (2017). http://dx.doi.org/10.4172/2375-4427.1000175.

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46

Salles, Frederico, and Betty McMicken. "Congenital Aglossia and the Report by Antoine de Jussieu: A Critical and Historical Review." Journal of Communication Disorders, Deaf Studies & Hearing Aids 4, no. 2 (2016). http://dx.doi.org/10.4172/2375-4427.1000157.

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McMicken, Betty, and Margaret Vento-Wilson. "Articulatory Movement during Production of Lingua-Alveolar Stop Consonants in a Case of Congenital Aglossia." Journal of Communication Disorders, Deaf Studies & Hearing Aids 03, no. 04 (2015). http://dx.doi.org/10.4172/2375-4427.1000142.

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48

Mahood, Kristin, Long Wang, Betty L. McMicken, and Cheryl Rock. "Wine Flavor Perception in a Person with Isolated Congenital Aglossia, Naïve Wine Taster, and Sommelier." Journal of Communication Disorders, Deaf Studies & Hearing Aids 05, no. 02 (2017). http://dx.doi.org/10.4172/2375-4427.1000174.

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