# Perioperative Care of a Four-Year-Old Child With Teebi Hypertelorism Syndrome: A Rare Craniofacial Disorder

**Authors:** Eslam Abdelhady, Joseph D. Tobias

PMC · DOI: 10.14740/jmc5268 · 2026-03-04

## TL;DR

This paper describes the anesthetic care of a 4-year-old child with a rare craniofacial disorder called Teebi hypertelorism syndrome during a thoracic surgery.

## Contribution

The paper presents the first reported case of anesthetic management for a patient with Teebi hypertelorism syndrome.

## Key findings

- The patient had characteristic craniofacial features and systemic malformations consistent with Teebi hypertelorism syndrome.
- Perioperative care considerations included managing potential complications related to craniofacial and systemic abnormalities.
- The case highlights the importance of a multidisciplinary approach for anesthetic management in rare craniofacial disorders.

## Abstract

Teebi hypertelorism syndrome (THS) is a rare, autosomal dominant craniofacial malformation disorder, characterized by orbital hypertelorism and characteristic craniofacial features, including a prominent forehead, wide arched eyebrows, short broad nasal root and tip, a thin upper lip, and a small chin. In addition to the characteristic phenotypic traits, systemic malformations may involve the limbs, central nervous system, urogenital tract, uterus, umbilicus (omphalocele), or cardiac system. Most cases can now be attributed to pathogenic variants in the SPECC1L gene on chromosome 22q11.23, leading to what is known as SPECC1L-related hypertelorism syndrome, which is associated with disruption of a cytoskeletal cross-linking protein. This protein is crucial for normal craniofacial morphogenesis during neural crest cell migration and midline facial formation. To date, there are no previous reports of anesthetic care in a patient with THS. We present a 4-year-old child with THS who presented for anesthetic care during thoracic laminectomy and excision of an intradural mass. We explore the history and clinical presentation of the disorder, outline end-organ involvement, and discuss perioperative concerns.

## Linked entities

- **Genes:** SPECC1L (sperm antigen with calponin homology and coiled-coil domains 1 like) [NCBI Gene 23384]
- **Diseases:** Teebi hypertelorism syndrome (MONDO:0030639)

## Full-text entities

- **Genes:** SPECC1L (sperm antigen with calponin homology and coiled-coil domains 1 like) [NCBI Gene 23384] {aka CYTSA, GBBB2, OBLFC1, TBHS, TBHS1}
- **Diseases:** hypertelorism syndrome (MESH:D006972), Craniofacial Disorder (MESH:D019465), THS (MESH:C538387), systemic malformations (MESH:D009421), omphalocele (MESH:D006554)
- **Species:** Homo sapiens (human, species) [taxon 9606]

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Source: https://tomesphere.com/paper/PMC12978399