Yunis Varon syndrome

Also Known As:

Cleidocranial Dysplasia with Micrognathia, Absent Thumbs, and Distal Aphalangia; Cleidocranial dysplasia, micrognathia, absent thumbs, & distal aphalangia; Yunis-Varon 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
- Inborn Genetic Diseases: 11939
  - Genetic Skin Diseases: 47
    - Ectodermal Dysplasia: 505
      - Yunis Varon syndrome: 2
Skin and Connective Tissue Diseases
- Skin Diseases: 13127
  - Skin Abnormalities: 159
    - Ectodermal Dysplasia: 505
      - Yunis Varon syndrome: 2
  - Genetic Skin Diseases: 47
    - Ectodermal Dysplasia: 505
      - Yunis Varon syndrome: 2
Stomatognathic Diseases: 705
- Jaw Diseases: 15
  - Jaw Abnormalities: 10
    - Micrognathism: 338
      - Yunis Varon syndrome: 2
- Stomatognathic System Abnormalities
  - Maxillofacial Abnormalities: 10
    - Jaw Abnormalities: 10
      - Micrognathism: 338
        Yunis Varon syndrome: 2

Related Diseases

1.	Glycogen Storage Disease Type IIb
2.	Glycogen Storage Disease Type II (Pompe's Disease)
3.	Charcot-Marie-Tooth Disease (Peroneal Muscular Atrophy)
4.	Absent corpus callosum cataract immunodeficiency

Experts

1.	Boenzi, Sara: 1 article (01/2021)
2.	Catesini, Giulio: 1 article (01/2021)
3.	Coşkun, Turgay: 1 article (01/2021)
4.	Deodato, Federica: 1 article (01/2021)
5.	Dionisi-Vici, Carlo: 1 article (01/2021)
6.	Lay, Incilay: 1 article (01/2021)
7.	Olivieri, Giorgia: 1 article (01/2021)
8.	Rizzo, Cristiano: 1 article (01/2021)
9.	Sacchetti, Elisa: 1 article (01/2021)
10.	Semeraro, Michela: 1 article (01/2021)

Drugs and Biologics

Drugs and Important Biological Agents (IBA) related to Yunis Varon syndrome:

1.	GlycogenIBA 01/01/2021 - "Besides Pompe disease, the tetrasaccharide Glc4 was increased also in disorders of autophagy (Vici syndrome, Yunis-Varon syndrome, and Danon disease) presenting cardiomuscular involvement with glycogen storage. Overall, results showed a clear separation between patients and controls, both in urine and in DUS. "
2.	Phosphoinositide PhosphatasesIBA 02/15/2016 - "FIG4 is a phosphoinositide phosphatase that is mutated in several diseases including Charcot-Marie-Tooth Disease 4J (CMT4J) and Yunis-Varon syndrome (YVS). "