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Periorbital Outcomes and Vision Risk Stratification in Treacher Collins Syndrome.
Ng, Jinggang J; Zhong, Anny; Massenburg, Benjamin B; Binenbaum, Gil; Wu, Meagan; Romeo, Dominic J; Katowitz, William R; Swanson, Jordan W; Bartlett, Scott P; Taylor, Jesse A.
Affiliation
  • Ng JJ; Division of Plastic, Reconstructive, and Oral Surgery, Children's Hospital of Philadelphia, Philadelphia, PA.
  • Zhong A; Division of Ophthalmology, Children's Hospital of Philadelphia, Pennsylvania, PA.
  • Massenburg BB; Division of Plastic, Reconstructive, and Oral Surgery, Children's Hospital of Philadelphia, Philadelphia, PA.
  • Binenbaum G; Division of Ophthalmology, Children's Hospital of Philadelphia, Pennsylvania, PA.
  • Wu M; Division of Plastic, Reconstructive, and Oral Surgery, Children's Hospital of Philadelphia, Philadelphia, PA.
  • Romeo DJ; Division of Plastic, Reconstructive, and Oral Surgery, Children's Hospital of Philadelphia, Philadelphia, PA.
  • Katowitz WR; Division of Ophthalmology, Children's Hospital of Philadelphia, Pennsylvania, PA.
  • Swanson JW; Division of Plastic, Reconstructive, and Oral Surgery, Children's Hospital of Philadelphia, Philadelphia, PA.
  • Bartlett SP; Division of Plastic, Reconstructive, and Oral Surgery, Children's Hospital of Philadelphia, Philadelphia, PA.
  • Taylor JA; Division of Plastic, Reconstructive, and Oral Surgery, Children's Hospital of Philadelphia, Philadelphia, PA.
Plast Reconstr Surg ; 2024 May 24.
Article de En | MEDLINE | ID: mdl-38857421
ABSTRACT

BACKGROUND:

We examined ophthalmologic outcomes and periorbital management in patients with Treacher Collins syndrome (TCS).

METHODS:

A retrospective cohort study was performed of children with TCS treated from 2009 to 2023 at our center. Demographics and medical history were collected. Primary outcomes were periorbital findings, surgical burden, and visual acuity. Patients were stratified by risk of vision loss based on ophthalmologic findings.

RESULTS:

Among 50 subjects, mean follow-up was 10.5±5.9 years. Periorbital findings included downslanting palpebral fissures (100%), eyelash deficiency (70%), eyelid coloboma (54%), and significant refractive error (50%). Twenty (40%) individuals underwent 86 periorbital procedures, including lateral canthopexy (n=23 operations) and malar/zygomatic reconstruction/augmentation (n=20). Lateral canthopexies accompanied by malar fat grafting were less likely to require reoperation (0% versus 72%, p=0.004). Subjects with eyelid coloboma were more likely to have exposure keratopathy (30% versus 4%, p=0.020). Grouped by risk of vision loss, 58% were "High" risk, 18% were "Moderate", and 24% were "Low". Among 78 eyes of 39 subjects, vision was "Good" in 90%, "Fair" in 5%, and "Poor" in 6%. Vision risk grading was associated with visual acuity outcomes (n=29) (p=0.050).

CONCLUSIONS:

In assessing long-term ophthalmological outcomes, we noted good vision despite significant periorbital anomalies. Though most eyelid colobomas can be managed with lubrication, those threatening corneal integrity should be repaired in infancy. As timely intervention may prevent visual impairment, we recommend perinatal ophthalmologist evaluation for all children with TCS. Our proposed vision risk scale may serve as a helpful paradigm by which to contemplate vision-related issues.

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Langue: En Journal: Plast Reconstr Surg Année: 2024 Type de document: Article Pays d'affiliation: Panama Pays de publication: États-Unis d'Amérique

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Langue: En Journal: Plast Reconstr Surg Année: 2024 Type de document: Article Pays d'affiliation: Panama Pays de publication: États-Unis d'Amérique