What is infantile angiokeratoma syndrome?

summary

Angiokeratoma syndrome is also called Fabry syndrome, Anderson Fabry syndrome, sweeley klionsky syndrome, ruiter pompen syndrome, diffuse systemic angiokeratoma glycolipid deposition, hemorrhagic sarcoidosis and so on. Let's share my experience with you.

What is infantile angiokeratoma syndrome?

Onset of disease in childhood or adolescence, the earliest is 6 years old. There may be repeated fever, Hypohidrosis, limb burning like paresthesia, acromegaly pain, renal failure, and even cerebrovascular embolism. The lesions were mainly in the lower abdomen, thighs and scrotum with small red spots and papular purpura.

There are many symptoms of nervous system, such as paroxysmal burning pain and paresthesia of limbs caused by pathological changes of peripheral nerve, posterior root and posterior horn of spinal cord, and paroxysmal abdominal pain, vomiting, diarrhea, Hypohidrosis and high fever caused by autonomic nervous system involvement;

Cerebral vascular wall involvement can cause hemiplegia, aphasia, convulsions and other local symptoms; Pituitary and hypothalamus involvement may have endocrine abnormalities. Ocular symptoms were also more common, such as tortuous dilation of retinal vessels and conjunctival vessels, corneal opacity, eyelid edema, and vision was affected in severe cases. Kidney, heart, lung, bone and joint can appear corresponding symptoms.

matters needing attention

In the diet must also control the salt intake, do not eat spicy food such as coffee, strong tea, you can eat more cereals such as cereals, oats or soybeans, you can drink more water or milk, but do not drink carbonated drinks.