ACRODYSOSTOSIS & TREATMENT

SIGNS SYMPTOMS / DISEASES INDEX (A) / ACRODYSOSTOSIS & TREATMENT
Read about acrodysostosis medical facts: what is the definition of acrodysostosis, what are the signs and symptoms, medical treatment & how to treat acrodysostosis, information about the causes, testing, and related acrodysostosis diseases.

Definition: What is "acrodysostosis"?

ACRODYSOSTOSIS

Acrodysostosis also known as acrodysplasia, Arkless-Graham, or Maroteaux-Malamut is defined as a very rare inborn skeletal illness which is marked by defects on the bones of feet, hands & the nose. Retardation of the patient's learning & mental development is a common occurrence.

Symptoms & Signs

The most common characteristics of acrodysostosis are: mild to average growth retardation; mental defect; hearing defects; & recurrent infections of the middle ear. The most probable complications include: arthritis; carpal tunnel syndrome; & a worsening range of spinal, elbow or hand movements.

Treatment: How to Treat "acrodysostosis"?

The treatment depends greatly on the physical or cognitive defects that are present. Orthopedic treatment & early intervention that are accompanied with special education is highly recommended by most physicians. Genetic counseling could be done to aid with the diagnosis, assessment of the risks & also testing. It is highly advised that the health care provider be contacted immediately when the parents notice retardation on their child's growth or development. Any other forms of infant abnormalities should also be given immediate medical attention.

Causes

Most of the patients that are afflicted with acrodysostosis do not have a family history of the illness. Sometimes, though, the disease can be inherited by the child from its parent as an autosomal dominant trait which means that the parents have the condition & they have passed it on to their offspring (even when the condition is apparent with just one of the two parents, this illness could still be inherited). Although it is now clear that the illness is caused by an inherited condition, to this day, the specific gene that causes the disease is still unrecognized.

Testing

A thorough physical examination would confirm the signs & symptoms of this illness. The findings could include: short stature; growth delays that can progress; hypertelorism or eyes that are wide-spaced; abnormal facial & head (craniofacial) features; a small & abnormally upturned nose which is characterized by a nasal bridge that appears flat; legs & arms that are shortened by defects of the feet & hands; defects on the genitals, skin, skeleton & teeth; & protrusion of the jaw. X-rays, on the first few months of life, could show stippling or mottled calcium deposits (especially on the nose). Infants may manifest short bones, an early growth of the hand & feet bones; shortened bones of the forearm (which are near the wrist); & unusually short toes & fingers also called brachydactyly.



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