Comparison of Resilience and Subjective Well-being to Fathers and Mothers Who Have Postlingual Deafness Children by Destalya Anggrainy Mogot Pandin, Efi Fitriana, Aulia Iskandarsyah, Juke Siregar

“…This study aims to compare the resilience and subjective well-being of fathers with mothers who have postlingual deafness children. Participants in this study were 336 parents (168 fathers and 168 mothers) who had postlingual deafness children, were biological fathers and mothers of postlingual deafness children, lived with their partners and children who experienced postlingual deafness, were able to communicate verbally and in writing using Indonesian good, domiciled in West Java. …”
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NLRP3 Is Expressed in the Spiral Ganglion Neurons and Associated with Both Syndromic and Nonsyndromic Sensorineural Deafness by Penghui Chen, Longxia He, Xiuhong Pang, Xiaowen Wang, Tao Yang, Hao Wu

“…Nonsyndromic deafness is genetically heterogeneous but phenotypically similar among many cases. …”
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Malay Version of Nijmegen Cochlear Implant Questionnaire and Quality of Life of Patients with Post-lingual Deafness by Mark PAUL, Asma ABDULLAH, Noor Dina HASHIM, Nur Fadhilah Megat ISMAIL, Shamsul Azhar SHAH

“…Phase II involves QOL assessment of post-lingual deafness using NCIQ-M. Results: Twenty CI users and 20 non-CI users answered the NCIQ-M. …”
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South African parents’ views on oral, signing, and bilingual communication for Deaf or hard-of-hearing children by Katijah Khoza-Shangase, Jasmine Bent

Subjects: “…deaf and hard-of-hearing (dhh) children…”
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CIP: an alternative career guidance model to improve self-understanding and work understanding for deaf students by Endang Pudjiastuti Sartinah, Esa Nur Wahyuni, Eryana Fatimasari Retno Budiati

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Case Report: Craniofacial deafness hand syndrome with unusual cardiovascular symptoms and lack of holistic care by Samantha Saenz Hinojosa, Carlos Reyes-Silva, Kazuyoshi Hosomichi, Vanessa I. Romero

“…The unique association of Craniofacial-Deafness-Hand Syndrome with cardiovascular anomalies due to a PAX3 variation provides valuable insights into the genetic underpinnings of this rare condition.…”
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Genomic characteristics of a Streptococcus suis of ST353 resulting in severe endophthalmitis with bilateral deafness by Liang Shen, Yanfei Tong, Shichao Li, Yuda Chen, Ruhan A, Zhen Li, Wenling Wang, Lijuan Yin, Jiuming Zou, Ziyong Sun, Changcheng Wu, Wenjie Tan, Haijuan Wang

“…This study explored a rare instance of intraocular infection and bilateral deafness caused by S. suis and emphasized the importance of timely diagnosis and treatment to prevent disease progression. …”
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The effectiveness of the training protocol based on acceptance and commitment on psychological distress and parenting stress of mothers with deaf children by Fatemeh Nikkhoo, Somaiyeh Fathipoor

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Being ‘excluded from the world of sound’: Deafness, Invalidism and Resilience in Harriet Martineau’s Writings (1834–1855) by Manuela D’Amore

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A case report of autosomal dominant deafness type 2A potentially resulting in muscular dystrophy by Yongyu Yang, Meilian Wang, Yan Lu, Jinliang Wu

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Case Report: The first Korean familial case of BCAP31-related deafness, dystonia, and cerebral hypomyelination by Yoong-A Suh, Jisun Hwang, Go Hun Seo, Rin Khang, Jang Hoon Lee, Moon Sung Park, Young Bae Sohn

“…Deafness, dystonia, and central hypomyelination (DDCH) syndrome (OMIM #300475) is a rare X-linked genetic disorder characterized by developmental delays, deafness, central hypomyelination, and dystonia. …”
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Hearing Screening Combined with Target Gene Panel Testing Increased Etiological Diagnostic Yield in Deaf Children by Le Xie, Yue Qiu, Yuan Jin, Kai Xu, Xue Bai, Xiao-Zhou Liu, Xiao-Hui Wang, Sen Chen, Yu Sun

“…By analyzing the patients who received 127 gene panel testing, we found that 51 deaf children carried variants which were not included in 159 variant testing. …”
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Relationship between mindfulness and self-control in deaf individuals: mediating role of inner peace and moderating role of life experience by Tong-Ao Zeng, Meng Xu, Han Zhu, Fu-Xiang Li, Xuan-feng Duan, Wen-Jun An, Fu-Yi Yang

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The dynamic Colombian sign language dataset for basic conversation LSC70Mendeley Data by Jader Alejandro Muñoz Galindez, Leidy Verónica Villota Coral, Rubiel Vargas Cañas

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Erratum to “Endolymphatic Sac Enlargement in a Girl with a Novel Mutation for Distal Renal Tubular Acidosis and Severe Deafness” by Nikki Rink, Martin Bitzan, Gus O'Gorman, Mato Nagel, Elena Torban, Paul Goodyer

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GJB6-D13S1830 and GJB6-D13S1854 Deletions in Patients with non-Syndromic Prelingual Deafness by Mercedes Arceo Álvarez, Estela Morales Peralta, Yuledmi Perdomo Chacón, Teresa Collazo Mesa

“…<strong>Foundation:</strong> GJB6-D13S1830 and GJB6-D13S1854 deletions are pathogenic variants of the GJB6 gene, which has been shown to be the second cause of autosomal recessive non-syndromic deafness in Spain, where some of our ancestors come from. …”
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A novel frameshift variant of GATA3 (p.Ala17ProfsTer178) responsible for HDR syndrome in a Japanese family by Yutaka Hasegawa, Toshie Segawa, Ai Chida, Eriko Yoshida, Hirofumi Kinno, Hiraku Chiba, Tomoyasu Oda, Yoshihiko Takahashi, Koji Nata, Yasushi Ishigaki

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The influence of segmental errors and stress-placement errors on Polish listeners’ perceived degree of foreignaccentedness in non-native speech by Anna Borkowska

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First African case report of hypoparathyroidism, deafness and renal dysplasia (HDR) syndrome due to inverted duplication and deletion of chromosome 10p by Tumelo M. Satekge, Glenrose Rikhotso, Bianca Rossouw, Bronwyn Dillon, Fiona Baine-Savanhu

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Cochlear Implantation in Single-Sided Deafness and Asymmetric Hearing Loss: 12 Months Follow-up Results of a European Multicenter Evaluation by Thomas Wesarg, Antje Aschendorff, Regina Baumgaertel, Julia Böttcher, Liesbeth De Coninck, Ingeborg Dhooge, Ann Dierckx, Thomas Klenzner, Philipp Schörg, Georg Sprinzl, Freya Swinnen, Nicolas Verhaert, Annelies Vermeiren, Simone Volpert, Andrzej Zarowski, Arne Ernst

“…Background: People with single-sided deafness (SSD) or asymmetric hearing loss (AHL) have particular difficulty understanding speech in noisy listening situations and in sound localization. …”
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