Meet a teenage girl whose body is gradually turning into stone in Sichuan Province, China.
Ni Min is suffering from a rare condition that turns her muscles to solid bone - fibrodysplasia ossificans progressiva (FOP). The genetic mutation is also known as Stone Man Syndrome and, unfortunately, there is still no cure for it. Although there are less than six hundred cases of it across the globe, those suffering from it eventually die.
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Ni Min began showing Stone Man syndrome symptoms at the age of eight.[/caption]
The 14-year-old girl began showing symptoms at the age of eight, after several examinations tests showed she was suffering from the genetic mutation. Despite the depressing prognosis doctors and Ni’s family hope to delay the symptoms with medication, in a bid to prolong her life and slow down the effect of the rare disease.
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Unfortunately, patients usually die in their 40s when they can no longer breathe.[/caption]
Dr Zhang Keqin, who is leading Ni’s treatment, said: “At present her condition is not very serious and we have prescribed medicine for her. We will see how that goes over the next 6 months. Patients usually die in their 40s when they can no longer breathe because of the pressure on their lungs.”
[caption id="attachment_3762" align="aligncenter" width="392"]
The extra bone progressively restricts movement, forming a second skeleton that imprisons the body in bone.[/caption]
The disease causes bone to form in muscles, tendons, ligaments and other connective tissues. Over time, this extra bone restricts movement, forming a second skeleton that imprisons the body in bone. It results in a gruesome death when the cartilage holding the ribs together also solidifies, making it impossible to breathe and eventually the patient suffocates or suffers massive cardiac arrest.
Ni Min is suffering from a rare condition that turns her muscles to solid bone - fibrodysplasia ossificans progressiva (FOP). The genetic mutation is also known as Stone Man Syndrome and, unfortunately, there is still no cure for it. Although there are less than six hundred cases of it across the globe, those suffering from it eventually die.
[caption id="attachment_3760" align="aligncenter" width="620"]
Ni Min began showing Stone Man syndrome symptoms at the age of eight.[/caption]The 14-year-old girl began showing symptoms at the age of eight, after several examinations tests showed she was suffering from the genetic mutation. Despite the depressing prognosis doctors and Ni’s family hope to delay the symptoms with medication, in a bid to prolong her life and slow down the effect of the rare disease.
[caption id="attachment_3761" align="aligncenter" width="634"]
Unfortunately, patients usually die in their 40s when they can no longer breathe.[/caption]Dr Zhang Keqin, who is leading Ni’s treatment, said: “At present her condition is not very serious and we have prescribed medicine for her. We will see how that goes over the next 6 months. Patients usually die in their 40s when they can no longer breathe because of the pressure on their lungs.”
[caption id="attachment_3762" align="aligncenter" width="392"]
The extra bone progressively restricts movement, forming a second skeleton that imprisons the body in bone.[/caption]The disease causes bone to form in muscles, tendons, ligaments and other connective tissues. Over time, this extra bone restricts movement, forming a second skeleton that imprisons the body in bone. It results in a gruesome death when the cartilage holding the ribs together also solidifies, making it impossible to breathe and eventually the patient suffocates or suffers massive cardiac arrest.
