Hearing Loss in Children with 22q11.2 Deletion Syndrome.

22q11.2 deletion syndrome chronic otitis media hearing loss myringotomy tube placement pediatric

Journal

The Laryngoscope
ISSN: 1531-4995
Titre abrégé: Laryngoscope
Pays: United States
ID NLM: 8607378

Informations de publication

Date de publication:
21 Sep 2024
Historique:
revised: 16 08 2024
received: 24 05 2024
accepted: 05 09 2024
medline: 21 9 2024
pubmed: 21 9 2024
entrez: 21 9 2024
Statut: aheadofprint

Résumé

Hearing loss is considered common in children with 22q11.2 deletion syndrome (22q11.2DS), with a few prior studies reporting a 32%-78% prevalence; mild-moderate conductive hearing loss has been reported most commonly. Overall, however, there remains a paucity of data regarding the frequency, type, age, and progression of hearing loss in children with 22q11.2DS. Retrospective chart review was completed, and data combined for two large 22q centers. Inclusion criteria were children with 22q11.2DS and a documented audiogram. Data extracted included a laboratory-confirmed chromosome 22q11.2 deletion; co-morbidities; results of all audiograms and radiologic temporal bone imaging; and otologic surgical procedures. One thousand seven hundred sixty-nine charts were reviewed; 775 met inclusion criteria. Of these, 563 (73%) children had at least one abnormal audiogram demonstrating hearing loss. A total of 2,536 audiograms were reviewed; 74% of these showed abnormal hearing in at least one ear. Most of the hearing loss was conductive (right ear 76%; left ear 69%) and mild severity. For the children with SNHL, 90% of all follow-up audiograms were stable without progression. Hearing loss was identified across all pediatric age ranges. Ear tube placement occurred in 39% of children. This study confirms the high incidence of hearing loss for children with 22q11.2DS at some point in their childhood. In our cohort, hearing loss occurred in 73% of children and was most often conductive and mild in severity. The results highlight the importance of otolaryngology and audiology involvement in managing children with 22q11.2DS for timely diagnosis and treatment of hearing loss. 4 Laryngoscope, 2024.

Identifiants

pubmed: 39305214
doi: 10.1002/lary.31777
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© 2024 The American Laryngological, Rhinological and Otological Society, Inc.

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Auteurs

Jill Arganbright (J)

Division of Pediatric Otolaryngology, Children's Mercy Hospital, Kansas, Missouri, U.S.A.
University of Missouri-Kansas City School of Medicine, Kansas, Missouri, U.S.A.

Terrence Blaine Crowley (TB)

22q and You Center, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, U.S.A.
Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, U.S.A.

Meghan Tracy (M)

Division of Pediatric Otolaryngology, Children's Mercy Hospital, Kansas, Missouri, U.S.A.

Janelle Noel-MacDonnell (J)

University of Missouri-Kansas City School of Medicine, Kansas, Missouri, U.S.A.
Health Services and Outcomes Research, Children's Mercy Hospital, Kansas, Missouri, U.S.A.

Kim Gaiser (K)

22q and You Center, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, U.S.A.
Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, U.S.A.

Lori Yaktine (L)

Division of Hearing and Speech, Children's Mercy Hospital, Kansas, Missouri, U.S.A.

Amanda Moore (A)

Division of Hearing and Speech, Children's Mercy Hospital, Kansas, Missouri, U.S.A.

Jamie Hamm (J)

Division of Hearing and Speech, Children's Mercy Hospital, Kansas, Missouri, U.S.A.

Bernice Morrow (B)

Albert Einstein Collect of Medicine, Bronx, New York, U.S.A.

Hansoo Song (H)

Albert Einstein Collect of Medicine, Bronx, New York, U.S.A.

Victoria Giunta (V)

22q and You Center, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, U.S.A.
Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, U.S.A.

Daniel E McGinn (DE)

22q and You Center, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, U.S.A.
Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, U.S.A.

Elaine H Zackai (EH)

22q and You Center, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, U.S.A.
Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, U.S.A.
Department of Pediatrics, Perelman School of Medicine of the University of Pennsylvania, Philadelphia, Pennsylvania, U.S.A.

Beverly Emanuel (B)

22q and You Center, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, U.S.A.
Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, U.S.A.
Department of Pediatrics, Perelman School of Medicine of the University of Pennsylvania, Philadelphia, Pennsylvania, U.S.A.

Lisa Elden (L)

22q and You Center, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, U.S.A.
Department of Surgery, Perelman School of Medicine of the University of Pennsylvania, Philadelphia, Pennsylvania, U.S.A.
Division of Otolaryngology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, U.S.A.

Srivats Narayanan (S)

University of Missouri-Kansas City School of Medicine, Kansas, Missouri, U.S.A.

Nikita Raje (N)

Division of Pediatric Allergy, Asthma, & Immunology, Children's Mercy Hospital, Kansas, Missouri, U.S.A.

Donna M McDonald-McGinn (DM)

22q and You Center, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, U.S.A.
Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, U.S.A.
Department of Pediatrics, Perelman School of Medicine of the University of Pennsylvania, Philadelphia, Pennsylvania, U.S.A.
Division of Human Biology and Medical Genetics, Sapienza, University, Rome, Italy.

Classifications MeSH