It occurs due to sporadic mutations in the majority of cases but can be inherited as an autosomal dominant condition. Homozygous achondroplasia is lethal.
There is a prevalence of approximately 1 in 25,000-50,000 births with males affected more frequently than females.
Achondroplasia is the most common cause of short-limb dwarfism. Patients are of normal intelligence with normal motor function. However, they may have specific neurologic deficits.
The disease results from a mutation in the fibroblast growth factor gene 3 (FGFR3) located on chromosome 4p16.3 which causes abnormal cartilage formation. All bones that form by endochondral ossification are affected. Bones that form by membranous ossification are not affected, thus allowing the skull vault to develop normally.
- SADDAN syndrome: severe achondroplasia with developmental delay and acanthosis nigricans
Almost all the bones of the skeleton are affected, and hence all parts of the body have bony changes with secondary soft tissue changes. Antenatally it is difficult to diagnose achondroplastic features until the 3rd trimester 13.
Antenatally detectable sonographic features include:
- short femur length measurement: often well below the 5th centile
- the femur length (FL) to biparietal diameter (BPD) is taken as a useful measurement
- trident hand 11: 2,3 and 4 fingers appearing separated and similar in length
- separation of 1st, 2nd, 3rd and 4th fingers
- protruding forehead: frontal bossing
- depressed nasal bridge
Features on radiographs, CT, and MRI are similar and discussed together here.
- relatively large cranial vault with small skull base
- prominent forehead with the depressed nasal bridge
- narrowed foramen magnum
- cervico-medullary kink
- relative elevation of the brainstem resulting in a large suprasellar cistern and vertically-oriented straight sinus
- communicating hydrocephalus (due to venous obstruction at sigmoid sinus)
Also, see the achondroplastic base of skull abnormalities for further discussion.
- posterior vertebral scalloping
- progressive decrease in the interpedicular distance in the lumbar spine
- gibbus: thoracolumbar kyphosis with bullet-shaped/hypoplastic vertebra (not to be confused with Hurler syndrome)
- short pedicle canal stenosis
- laminar thickening
- widening of intervertebral discs 8
- an increased angle between the sacrum and lumbar spine
- anterior flaring of the ribs
- anteroposterior narrowing of the ribs
Pelvis and hips
- horizontal acetabular roof (decreased acetabular angle)
- small squared (tombstone or mickey mouse ear) iliac wings
- small trident pelvis
- champagne glass type pelvic inlet
- short sacroiliac notches
- metaphyseal flaring 8: can give a trumpet bone type appearance
- the femora and humeri are particularly shortened (rhizomelic shortening)
- long fibula: the fibular head is at the level of the tibial plateau (case 3)
- the limbs may also appear thickened but are in fact normal in absolute terms; thickening is perceived due to reduced length
- trident hand
- chevron sign 16,17
- the metacarpal and metatarsal bones, and in some cases the proximal phalanges, are short and of similar length
Treatment and prognosis
There is often a danger of cervical cord compression due to narrowing of the foramen magnum.
Treatment varies and is usually orthopedic, particularly to correct kyphoscolioses, as well as neurosurgical, to decompress the foramen magnum or shunt hydrocephalus 6-7.
Overall prognosis is good, with near-normal life expectancy in heterozygous individuals. When homozygous, the condition is fatal due to respiratory failure 7.
History and etymology
Achondroplasia literally means "without cartilage formation", although the pathology is impaired endochondral ossification (see Pathology above).
The differential diagnosis is that of other less common skeletal dysplasias, including 6:
- campomelic dysplasia
- thanatophoric dysplasia
- chondroectodermal dysplasia (Ellis-van Creveld syndrome)
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