Hypochondroplasia
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Through Dominance (genetics), Birth and Embryo
Signs and symptoms
Individuals affected by this disorder appear normal at birth. As the infant grows, however, their arms and legs do not develop properly, and their body becomes thicker and shorter than normal. The following are characteristics consistent with this condition:
- Brachydactyly
- Short stature
- Micromelia
- Skeletal dysplasia
- Abnormality of femur
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Cause
Hypochondroplasia is inherited as an autosomal dominant trait affecting the FGFR3 gene on chromosome 4p16.3. There is currently no cure for this condition.
Pathophysiology
This disorder results from mutations in the proximal tyrosine kinase domain of the FGFR3 gene. This gene plays an important role in embryonic development, helping to regulate activities such as cell division, migration and differentiation.
Hypochondroplasia can be caused by point mutations such as p. Lys650Asn. In FGFR3, some 20 different mutations have been associated with hypochondroplasia, and it seems to have a role in skeletal dysplasia.
Diagnosis
The diagnosis of this condition can be done via X-rays (with lack of normal distance L1 to L5), and additionally genetic testing is available to ascertain hypochondroplasia. However, the physical characteristics are one of the most important in determining the condition.
Treatment
Treatment of hypochondroplasia usually takes the form of orthopedic surgery and physical therapy. Genetic counseling is advised for individuals and their families. Specifically in the case of spinal stenosis, one option is laminectomy.
Prognosis
Life expectancy for individuals with hypochondroplasia is normal; height is about 132–147 centimetres (4 ft 4 in – 4 ft 10 in).