Syndrome de Hay-Wells : à propos d’un cas

Khalfi, Lahcen; Hamama, Jalal; Mahroug, Layla; Adil, A.; Sabani, Hicham

doi:10.1016/j.arcped.2015.11.016

Cited by 3 publications

(1 citation statement)

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“…AEC syndrome was first reported by Hay and Wells in 1976 and is considered to be a rare type of ectodermal dysplasia. 7 Ankyloblepharon is usually limited to small bands of vascularized connective tissue spanning the eyelids, and such is the classical feature that distinguishes AEC syndrome from other disorders that also present with ectodermal dysplasia and cleft palate and/or lip. 3 Diagnosis is based on the characteristic symptoms, a detailed history, and a thorough clinical evaluation.…”

Section: Discussionmentioning

confidence: 99%

Two Airway Management Techniques in a Pediatric Patient with Temporomandibular Joint Ankylosis: Two-stage Fiberoptic Scope Intubation Technique and Video Laryngoscope-guided Conversion from Nasotracheal to Orotracheal Intubation — A Case Report

Manera

Hilvano-Corsiga

2022

Acta Med Philipp

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Ankyloblepharon-ectodermal dysplasia-clefting (AEC) syndrome is an ectodermal dysplasia presenting with cleft lip or palate and congenital filiform eyelid fusion. This is a case report of a 1-year and 6-month-old girl with AEC syndrome presenting with temporomandibular joint ankylosis who underwent release of temporomandibular joint ankylosis, coronoidectomy, bilateral cheiloplasty, Tajima rhinoplasty, and repair of lower lip pits under general anesthesia. Fiberoptic nasotracheal intubation was done successfully using a two-stage technique originally described by Stiles. As necessitated by the surgical plan, video laryngoscope guidance was subsequently used to facilitate the conversion from nasotracheal to orotracheal intubation.

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Section: Discussionmentioning

confidence: 99%