RIDDLE syndrome
Medical condition
From Wikipedia, the free encyclopedia
RIDDLE syndrome is a rare genetic syndrome. The name is an acronym for Radiosensitivity, ImmunoDeficiency Dysmorphic features and Learning difficulties.
| RIDDLE syndrome | |
|---|---|
| Other names | Radiosensitivity-immunodeficiency-dysmorphic features-learning difficulties syndrome |
 | |
| Riddle syndrome is inherited in an autosomal recessive pattern. | |
Presentation
The features of this condition include:[citation needed]
- Facial dysmorphism
- Short stature
- Mild motor control and learning difficulties
- Mild ataxia
- Microcephaly
- Normal intelligence
- Conjunctival telangiectasia
- Recurrent sinus infections
- Decreased serum IgA
- Late onset of pulmonary fibrosis
- Increased alpha-fetoprotein
- Increased radiosensitivity
Genetics
This condition is due to mutations in the RNF168 gene. It is inherited in an autosomal recessive fashion. The gene encodes a ubiquitin ligase and is located on the long arm of chromosome 3 (3q29) on the Crick (minus strand).[1]
Diagnosis
Differential diagnosis
The DDx is [citation needed]
Management
Epidemiology
This condition is extremely rare. Only four cases have been described up to 2017.[2]
History
This syndrome was first described by Stewart et al. 2007.[3]