| Kaufman oculocerebrofacial syndrome | |
|---|---|
| Other names | Blepharophimosis-ptosis-intellectual disability syndrome |
 | |
| Kaufman oculocerebrofacial syndrome has an autosomal recessive pattern of inheritance. | |
| Symptoms | Arachnodactyly |
| Causes | Mutation in the UBE3B gene |
| Diagnostic method | Growth assessment, Thyroid function evaluation |
| Treatment | Thyroid hormone replacement, Speech therapy |
Kaufman oculocerebrofacial syndrome is an autosomal recessive congenital disorder characterized by mental retardation, brachycephaly, upslanting palpebral fissures, eye abnormalities, and highly arched palate. It was characterized in 1971; eight cases had been identified as of 1995.
Symptoms and signs
The signs and symptoms of Kaufman oculocerebrofacial syndrome are consistent with the following:
- High palate
- Microcephaly
- Constipation
- Intellectual disability
- Muscular hypotonia
- Nystagmus
Cause
The cause of this condition is apparently due to mutation in the UBE3B gene and is inherited via autosomal recessive manner. This gene is located at molecular location- base pairs 109,477,410 to 109,543,628 and position 24.11 on chromosome 12.
Genetics
The mechanism (or pathogenesis) of Kaufman oculocerebrofacial syndrome appears to begin due to a mutation in the E3 ubiquitin protein ligase. (UBE3B).
One finds that the normal mechanism of UBE3B gene is important in the ubiquitin-proteasome system. The aforementioned system helps to remove proteins that have degraded.
However, when not working properly due to the mutation in the UBE3B gene(at least 15 mutations) results in an unstable UBE3B protein which has a negative effect on the ubiquitin-proteasome system.
Diagnosis
The diagnosis of Kaufman oculocerebrofacial syndrome can be achieved via molecular testing approaches. Additionally to ascertain if the individual has the condition:
- Growth assessment
- Thyroid function evaluation
- Kidney ultrasound
- Echocardiogram
Differential diagnosis
Kaufman oculocerebrofacial syndrome differential diagnosis consists of:
- Ohdo syndrome
- Smith–Lemli–Opitz syndrome
- Maat–Kievit–Brunner syndrome
- Chromosome 3pter-p25 deletion syndrome
Management
Treatment for this condition entails surveillance of growth and contractures. Furthermore, the following are treatment options:
See also
Further reading
- Pryse-Phillips, William (2009). Companion to clinical neurology (3rd ed.). Oxford: Oxford University Press. ISBN 9780195367720. Retrieved 29 July 2017.
- al.], Victor A. McKusick; with the assistance of Stylianos E. Antonarakis ... [et (1997). Mendelian inheritance in man : a catalog of human genes ... (12. ed.). Baltimore, Md.: Johns Hopkins. ISBN 9780801857423. Retrieved 29 July 2017.