Human Growth Foundation

Headquarters:

997 Glen Cove Ave, Suite 5

Glen Head, New York 11545 USA

Email: hgf1@hgfound.org

Telephone: 1-800-451-6434

Fax Number: 1-516-671-4055

Human Growth Foundation (HGF)

is a  501(c)(3) non-profit organization.

 

Federal Tax Identification# 16-0913012  

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XLH (X-Linked Hypophosphatemia)

X-linked hypophosphatemia (XLH) is an inherited disorder characterized by low levels of phosphate in the blood.

 

Phosphate levels are low because phosphate is abnormally processed in the kidneys, which causes a loss of phosphate in the urine (phosphate wasting) and leads to soft, weak bones (rickets).

 

XLH is usually diagnosed in childhood. Features include bowed or bent legs, short stature, bone pain, and severe dental pain.

 

XLH is caused by mutations in the PHEX gene on the X chromosome, and inheritance is X-linked dominant. Treatment generally involves supplements of phosphate and high-dose calcitriol (the active form of Vitamin D), and may also include growth hormones, corrective surgery, and dental treatment. The long-term outlook varies depending on the severity and whether complications arise. While some adults with XLH may have minimal medical problems, others may experience persistent discomfort or complications.