HOME PRODUCTS COMPANY CONTACT FAQ

Research Dictionary Pharma

Sign Up FREE or Login

Pierre Robin syndrome with fetal chondrodysplasia

Also Known As:

Heterozygous Osmed; Heterozygous Otospondylomegaepiphyseal Dysplasia; Weissenbacher-Zweymuller syndrome; Weissenbacher-Zweymüller Syndrome

Networked: 2 relevant articles (0 outcomes, 0 trials/studies)

Disease Context: Research Results

Musculoskeletal Diseases: 719
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
- Congenital Abnormalities: 25723
  - Musculoskeletal Abnormalities: 43
    - Craniofacial Abnormalities: 203
      - Maxillofacial Abnormalities: 10
        Jaw Abnormalities: 10
        Pierre Robin Syndrome: 349
        Pierre Robin syndrome with fetal chondrodysplasia: 2
  - Stomatognathic System Abnormalities
    - Maxillofacial Abnormalities: 10
      - Jaw Abnormalities: 10
        Pierre Robin Syndrome: 349
        Pierre Robin syndrome with fetal chondrodysplasia: 2
- Inborn Genetic Diseases: 11939
  - Osteochondrodysplasias: 592
    - Pierre Robin syndrome with fetal chondrodysplasia: 2
Stomatognathic Diseases: 705
- Jaw Diseases: 15
  - Jaw Abnormalities: 10
    - Pierre Robin Syndrome: 349
      - Pierre Robin syndrome with fetal chondrodysplasia: 2
- Stomatognathic System Abnormalities
  - Maxillofacial Abnormalities: 10
    - Jaw Abnormalities: 10
      - Pierre Robin Syndrome: 349
        Pierre Robin syndrome with fetal chondrodysplasia: 2

Related Diseases

1.	Pierre Robin syndrome with fetal chondrodysplasia
2.	type 3 Stickler syndrome
3.	type 1 Stickler syndrome
4.	Megaepiphyseal dwarfism

Experts

1.	Bademci, Guney: 1 article (08/2015)
2.	Bensaid, Mariem: 1 article (08/2015)
3.	Chakchouk, Imen: 1 article (08/2015)
4.	Chakroun, Amine: 1 article (08/2015)
5.	Diaz-Horta, Oscar: 1 article (08/2015)
6.	Duman, Duygu: 1 article (08/2015)
7.	Farooq, Amjad: 1 article (08/2015)
8.	Foster, Joseph: 1 article (08/2015)
9.	Ghorbel, Abdelmonem: 1 article (08/2015)
10.	Grati, M'hamed: 1 article (08/2015)

Drugs and Biologics

Drugs and Important Biological Agents (IBA) related to Pierre Robin syndrome with fetal chondrodysplasia:

1.	Collagen Type XIIBA 08/01/2015 - "HL due to mutations in COL11A2, encoding collagen type XI alpha-2, can be non-syndromic autosomal-dominant or autosomal-recessive, and also syndromic as in Otospondylomegaepiphyseal Dysplasia, Stickler syndrome type III, and Weissenbacher-Zweymuller syndrome. "
2.	Glycine (Aminoacetic Acid)FDA LinkGeneric 11/02/1998 - "Heterozygous glycine substitution in the COL11A2 gene in the original patient with the Weissenbacher-Zweymüller syndrome demonstrates its identity with heterozygous OSMED (nonocular Stickler syndrome)."