Javascript must be enabled to continue!
Apert Syndrome Type III Hand: Prevalence and Outcomes
View through CrossRef
Background:
The Upton type III hand, which represents the most severe hand type among Apert syndrome patients, has been considered the least prevalent hand type. The objective of this study is to address type III Apert hand prevalence and describe treatment strategies that will result in a 5 digit hand.
Methods:
The authors retrospectively reviewed 15 years of Apert syndrome hand practice at our hospital. Demographic (patient sex and age at the time of the operation), surgical (eg, techniques used for webspace release, osteotomy, and various aspects of soft-tissue reconstruction), and outcome (perioperative and long-term complication and need for revision operation) data was verified through medical records, clinical photographs, radiographic images, and interviews with patients’ families. Patients who had incomplete medical records and/or postoperative follow up <6 months in length were excluded from this study.
Results:
A total of 93 Apert patients [50 male (56.1%) and 43 female (43.9%)] were treated at our hospital from 2007 to 2021. Stratification of Apert hand severity using Upton’s classification system identified 34 patients with type I hands (36.4%), 19 patients with type II hands (20.6%), and 40 patients with type III hands (43%). Of the 40 patients with type III hands a 5 digit hand was achieved for 35 patients (87%), with an average of 3.37 operations per patient.
Conclusions:
The Upton type III hand is the most prevalent hand type among Apert syndrome patients. Following a three stage protocol, a surgical team can consistently achieve a 5 digit hand for the majority of Apert syndrome patients with type III hands.
Ovid Technologies (Wolters Kluwer Health)
Title: Apert Syndrome Type III Hand: Prevalence and Outcomes
Description:
Background:
The Upton type III hand, which represents the most severe hand type among Apert syndrome patients, has been considered the least prevalent hand type.
The objective of this study is to address type III Apert hand prevalence and describe treatment strategies that will result in a 5 digit hand.
Methods:
The authors retrospectively reviewed 15 years of Apert syndrome hand practice at our hospital.
Demographic (patient sex and age at the time of the operation), surgical (eg, techniques used for webspace release, osteotomy, and various aspects of soft-tissue reconstruction), and outcome (perioperative and long-term complication and need for revision operation) data was verified through medical records, clinical photographs, radiographic images, and interviews with patients’ families.
Patients who had incomplete medical records and/or postoperative follow up <6 months in length were excluded from this study.
Results:
A total of 93 Apert patients [50 male (56.
1%) and 43 female (43.
9%)] were treated at our hospital from 2007 to 2021.
Stratification of Apert hand severity using Upton’s classification system identified 34 patients with type I hands (36.
4%), 19 patients with type II hands (20.
6%), and 40 patients with type III hands (43%).
Of the 40 patients with type III hands a 5 digit hand was achieved for 35 patients (87%), with an average of 3.
37 operations per patient.
Conclusions:
The Upton type III hand is the most prevalent hand type among Apert syndrome patients.
Following a three stage protocol, a surgical team can consistently achieve a 5 digit hand for the majority of Apert syndrome patients with type III hands.
Related Results
The APERT Severity Scale: A Quantitative Tool for Risk Stratification in Apert Syndrome
The APERT Severity Scale: A Quantitative Tool for Risk Stratification in Apert Syndrome
Introduction:
Apert syndrome is a rare congenital disorder caused by FGFR2 mutations, characterized by craniosynostosis, midface hypoplasia, and syndactyly. The...
Treatment of Apert Hand Syndrome: Strategies for Achieving a Five-Digit Hand
Treatment of Apert Hand Syndrome: Strategies for Achieving a Five-Digit Hand
Background:
Apert hand reconstruction requires complex surgical planning. The purpose of this study was to describe the authors’ 8-year surgical experience with Apert s...
Abnormalities Detection in Apert Syndrome using Hierarchical Clustering Algorithms
Abnormalities Detection in Apert Syndrome using Hierarchical Clustering Algorithms
Craniosynostosis syndrome is a congenital condition occurring due to the abnormal development of the skull, leading to abnormalities in skull morphology. Apert syndrome is one of c...
Management of hearing loss in Apert syndrome
Management of hearing loss in Apert syndrome
Background: Apert syndrome is one of the craniosynostosis syndromes, with abirth prevalence estimated to be between 9.9 and 15.5/million, and accounts for 4.5 per cent ofcraniosyno...
Posterior vault distraction osteogenesis in Apert syndrome
Posterior vault distraction osteogenesis in Apert syndrome
Apert syndrome is an uncommon autosomal dominant condition with a varied clinical spectrum which includes premature cranial and facial suture fusion and complex upper and lower li...
Apert syndrome: A dermatologist’s perspective
Apert syndrome: A dermatologist’s perspective
Apert syndrome is a Type 1 acrocephalosyndactyly syndrome presenting predominantly with craniofacial malformations and syndactyly. It can present with a multitude of clinical featu...
Facial Fat Graft Injection Reduces Asymmetry and Improves Forehead Contour in Early Infancy Apert Syndrome Patients
Facial Fat Graft Injection Reduces Asymmetry and Improves Forehead Contour in Early Infancy Apert Syndrome Patients
Background:
The objective of this study is to report the outcomes of a modified comprehensive Apert syndrome surgical protocol in which fat injection was performed duri...
SINDROME DE APERT ASSOCIADA A PERSISTÊNCIA DO CISTO DE BLAKE: UMA ASSOCIAÇÃO CLÍNICA RARA
SINDROME DE APERT ASSOCIADA A PERSISTÊNCIA DO CISTO DE BLAKE: UMA ASSOCIAÇÃO CLÍNICA RARA
A Síndrome Apert é uma doença genética rara que pode ser chamada também de acrocefalossindactilia. É definida geneticamente como doença hereditária autossômica dominante relacionad...

