Congenital Hand and Upper Extremity Malformations

NCT ID: NCT05182333

Last Updated: 2022-01-10

Basic Information

• Recruitment Status: UNKNOWN
• Total Enrollment: 100 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2022-02-01
• Study Completion Date: 2022-07-01

Brief Summary

Getting the incidence of upper limb anomalies in our department from 2000 to 2020 and classifying them using IFSSH classification and OMT classification

Detailed Description

A retrospective look at the past 20 years illustrated the changes and developments that characterize the world of hand surgery. During these years, old techniques were developed and standardized, new surgical techniques were described, our knowledge improved and illustrated by better classification systems, and new ideas were born that would guide the future of hand surgery. Limb deformities are among the most common birth defects in infants. Over the past 150 years, many classifications of limb abnormalities based on bone morphology and anatomy have been developed.

Congenital anomalies of the hand require consistent and reproducible terminology, and it is a universal language that allows discussion of complex clinical entities, treatment indications and outcome comparisons.

Ideally, the classification of congenital anomalies of the hand will depend on the etiology, giving some indication of the location in the molecular pathway and / or the anatomical location in the developing limb bud where the error occurs and the moment when the fault occurs. The terms should be understandable to geneticists, anatomists, pathologists, and surgeons, and they should allow easy interpretation to parents and, where appropriate, children affected by these conditions. The classification of congenital anomalies of the upper extremity and the important association of these anomalies with systemic disorders and syndromes are described in this study. Depending on the classification, examples are given for each class of anomalies.

Conditions

Congenital Limb Anomaly Nos

Study Design

• Observational Model Type: CASE_CONTROL
• Study Time Perspective: RETROSPECTIVE

Interventions

Examination

History taking, examination of upper limb

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

• All patients with congenital upper limb anomalies in last 20 years in Assiut university hospital.

Exclusion Criteria

• Conditions that were considered to be difficult to correctly classify because of late presentation, a large span of clinical presentation, extremely rare conditions, and conditions difficult to differentiate from traumatic conditions were excluded (ie, congenital radial head dislocation, congenital tumorous conditions, Marfan syndrome)

• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Assiut University

OTHER

Sponsor Role: lead

Responsible Party

Shady Magdy Makar Salieb

Principle investigator

Responsibility Role: PRINCIPAL_INVESTIGATOR

Central Contacts

Shady Salieb, MD

Role: CONTACT

shadymagdy93@gmail.com

+201028700865

Mostafa El-Sonbati, Professor

Role: CONTACT

mostafaelsonbati1@med.aun.edu.eg

+201003142066

References

McCarroll HR. Congenital anomalies: a 25-year overview. J Hand Surg Am. 2000 Nov;25(6):1007-37. doi: 10.1053/jhsu.2000.6457.

Reference Type: BACKGROUND

PMID: 11119659 (View on PubMed)

Tayel SM, Fawzia MM, Al-Naqeeb NA, Gouda S, Al Awadi SA, Naguib KK. A morpho-etiological description of congenital limb anomalies. Ann Saudi Med. 2005 May-Jun;25(3):219-27. doi: 10.5144/0256-4947.2005.219.

Reference Type: BACKGROUND

PMID: 16119523 (View on PubMed)

Other Identifiers

Congenital UL anomalies

Identifier Type: -

Identifier Source: org_study_id