About Autosomal Recessive Hypophosphatemic Rickets

Hypophosphatemic Rickets, Autosomal Recessive, 1, also known as hypophosphatemic rickets, ar, is related to hypophosphatemic rickets, autosomal recessive, 2 and dentinogenesis imperfecta. An important gene associated with Hypophosphatemic Rickets, Autosomal Recessive, 1 is DMP1 (Dentin Matrix Acidic Phosphoprotein 1). Affiliated tissues include bone, skeletal muscle and heart, and related phenotypes are sensorineural hearing impairment and hypophosphatemia

Major Symptoms of Autosomal Recessive Hypophosphatemic Rickets

Hypophosphatmic rickets is an inherited disorder caused by a deficiency of vitamin D, calcium, or phosphorus. Some of the major symptoms include bowing of the legs, a wide wrist, and a deformity of the chest and pelvis. It can also cause calcification of the eyes, hearing, and teeth. In addition, it may lead to low bone density and an increased risk of osteoporosis.

Suitable Lifestyle for People with Autosomal Recessive Hypophosphatemic Rickets

For patients with Autosomal recessive Hypophosphatmic rickets, that is, hereditary hypophosphatemia, it is recommended that their lifestyle should include the following points:

1. Dietary adjustment: Patients should avoid high-phosphorus foods, such as animal liver, fish, shrimp, and crabs , beans, etc. , while increasing the intake of vegetables, fruits and whole grain foods in an appropriate amount to supplement vitamin D and calcium.

2. Supplement vitamin D: Patients should receive regular sun exposure and appropriate vitamin D supplementation to help promote the absorption and utilization of calcium and phosphorus.

3. Maintain a good weight: Patients should avoid obesity to reduce the burden on their bones. If necessary, they can take measures such as diet control and exercise.

4. Avoid smoking and alcohol abuse: Smoking and alcohol abuse may have adverse effects on bone health, and patients should try to avoid these bad habits.

5. Carry out relevant examinations regularly: Patients should receive relevant examinations regularly, such as blood calcium and blood phosphorus levels, so that treatment plans can be adjusted in a timely manner.

6. Follow the doctor's advice: Patients should follow the doctor's treatment recommendations, take medications on time, and have regular check-ups. It should be noted that while patients adjust their lifestyle, they should also pay attention to changes in their condition, such as the relief and progression of symptoms, and report to their doctors in a timely manner.

Other Diseases

Hypophosphatemic Rickets Autosomal Recessive Bestrophinopathy Autosomal Recessive Polycystic Kidney Autosomal Recessive Congenital Ichthyosis Autosomal Recessive Isolated Ectopia Lentis Autosomal Recessive 1 Primary Hypertrophic Osteoarthropathy Autosomal Recessive Spastic Paraplegia Type 54 Autosomal Recessive Spastic Paraplegia Type 35 Autosomal Recessive 2 Primary Hypertrophic Osteoarthropathy Autosomal Recessive Early-Onset Parkinson Disease 6

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