Results 81 to 90 of about 28,866 (195)

Transoral Robotic Surgery Versus Traditional Lingual Tonsillectomy for Persistent Pediatric Sleep Apnea

Laryngoscope Investigative Otolaryngology, Volume 11, Issue 4, August 2026.
ABSTRACT Objectives This study compares postoperative outcomes of transoral robotic surgery (TORS) and traditional lingual tonsillectomy in pediatric patients with persistent obstructive sleep apnea (OSA) following tonsillectomy and adenoidectomy (T&A).
Mona Dabbas, Christina Zhu, Emily Clementi, Samay Sampat, Kristen Mathew, Earl Harley   +5 more
wiley   +1 more source

Clinical case seminar - Hypogonadotropic hypogonadism as a presenting feature of late-onset X-linked adrenal hypoplasia congenita [PDF]

, 2002
Mutations in the orphan nuclear receptor DAX-1 cause X-linked adrenal hypoplasia congenita. Affected boys usually present with primary adrenal failure in early infancy or childhood.
Beck-Peccoz, P, Achermann, JC, Romoli, R, Spada, A, Mantovani, G, Persani, L, Jameson, JL, Ozisik, G, Borretta, G   +8 more
core  

Craniofacial manifestations and dental considerations in association with achondroplasia: Clinical insight and report of a case

SRM Journal of Research in Dental Sciences, 2016
Achondroplasia is of clinical interest in dental practice because of its distinctive craniofacial features, which include relative macrocephaly, a short posterior cranial base, depressed nasal bridge, and maxillary hypoplasia. Treatment planning for such
Nidhi Chhabra, Anuj Chhabra, Ruchi Mehta
doaj   +1 more source

Identification and characterization of a highly conserved protein absent in the Alport S. (A), mental retardation (M), midface hypoplasia (M), and elliptocytosis (E) contiguous gene deletion syndrome

, 1999
We recently described a novel contiguous gene deletion syndrome (AMME) in Xq22.3 that includes Alport syndrome (A), mental retardation (M), midface hypoplasia (M), and elliptocytosis (E).
POBER, B., MALANDRINI, A., V. SORRENTINO, VITELLI, F., A. MALANDRINI, B. POBER, FRANCO, B., M. PICCINI, SORRENTINO, V., F. CAROLI, JONSSON, J., J. JONSSON, FRANCO, BRUNELLA, A. RENIERI, CAROLI, F., PICCINI, M., F. VITELLI, RENIERI, A.   +17 more
core   +1 more source

Apert syndrome and repercussions in Dental Medicine [PDF]

, 2020
Apert’s syndrome is a craniosynostosis syndrome caused by mutations in the gene coding for the fibroblast growthfactor receptor 2 (FGFR2), characterized by craniosynostosis, midface hypoplasia and syndactyly of the hands and feet.
Paula, Lígia de, Cardoso, Inês Lopes
core   +1 more source

Apert syndrome

Journal of Indian Society of Pedodontics and Preventive Dentistry, 2010
Apert syndrome (acrocephalosyndactyly) is a rare developmental malformation characterized by craniosynostosis, mid-face hypoplasia, symmetrical syndactyly of hands and feet. The prodromal characteristics for the typical cranio-facial appearance are early
Premalatha, Kannan V, Madhu
doaj  

Reply: Simultaneous Midface Advancement and Orthognathic Surgery: A Powerful Technique for Managing Midface Hypoplasia and Malocclusion

Plastic & Reconstructive Surgery, 2021
Erik M, Wolfswinkel, Laya, Jacob, Jeffrey A, Hammoudeh, Mark M, Urata   +3 more
openaire   +3 more sources

An alternate translation initiation site circumvents an amino-terminal DAX1 nonsense mutation leading to a mild form of X-linked adrenal hypoplasia congenita [PDF]

, 2003
Mutations in DAX1 [dosage-sensitive sex reversal-adrenal hypoplasia congenita (AHC) critical region on the X chromosome gene 1; NROB1] cause X-linked AHC, a disease characterized by primary adrenal failure in infancy or childhood and reproductive ...
Beck-Peccoz, P, J. L. Jameson, A. Spada, Spada, A, G. Mantovani, Weiss, J, P. Beck-Peccoz, Ozisik, G, L. Persani, Achermann, JC, Mantovani, G, J. C. Achermann, J. Weiss, Persani, L, Jameson, JL, G. Ozisik   +15 more
core   +1 more source

Evaluation of cephalometric points in midface bone lengthening with the use of a rigid external device in syndromic craniosynostosis patients Avaliação de pontos cefalométricos no alongamento ósseo do terço médio da face em portadores de craniossinostose sindrômica com a utilização de dispositivo externo rígido

Brazilian Journal of Otorhinolaryngology, 2009
Distraction osteogenesis has been extensively used to correct severe midface hypoplasia in syndromic craniosynostosis patients. However few studies have reported midface distraction outcomes through cephalometric evaluation.
Daniel Santos Corrêa Lima, Nivaldo Alonso, Paulo Roberto Pelúcio Câmara, Dov Charles Goldenberg   +3 more
doaj   +1 more source

Anesthetic Management of Cervicomedullary Decompression in a Child With Down Syndrome: A Case Report

Pediatric Discovery, Volume 4, Issue 3, September 2026.
Muhammad Saad, Marium Amjad
wiley   +1 more source