Camptodactyly syndrome Guadalajara type 1

Also Known As:

Camptodactyly Syndrome, Guadalajara, Type I; Facio-thoraco-skeletal syndrome; Faciothoracoskeletal Syndrome; Guadalajara camptodactyly syndrome; Guadalajara camptodactyly syndrome type 1

Networked: 1 relevant articles (0 outcomes, 0 trials/studies)

Disease Context: Research Results

Musculoskeletal Diseases: 719
- Hand Deformities: 72
  - Congenital Hand Deformities: 2
    - Camptodactyly syndrome Guadalajara type 1: 1
- Musculoskeletal Abnormalities: 43
  - Congenital Limb Deformities: 8
    - Congenital Upper Extremity Deformities
      - Congenital Hand Deformities: 2
        Camptodactyly syndrome Guadalajara type 1: 1
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
- Congenital Abnormalities: 25723
  - Musculoskeletal Abnormalities: 43
    - Congenital Limb Deformities: 8
      - Congenital Upper Extremity Deformities
        Congenital Hand Deformities: 2
        Camptodactyly syndrome Guadalajara type 1: 1

Drugs and Biologics

Drugs and Important Biological Agents (IBA) related to Camptodactyly syndrome Guadalajara type 1:

1.	goblet cell silencer inhibitorIBA 01/01/1993 - "Three sibs, two girls aged 18 and 9 years, and a 7-year-old boy, were found to have Guadalajara camptodactyly syndrome type I (GCSI). "