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Diseases Details

Treacher-Collins syndrome [View testimonials]
Treacher-Collins syndrome is a condition that is passed down through families (hereditary) and leads to defects of the face. Treacher Collins syndrome is a rare genetic disorder characterized by craniofacial deformities. Treacher Collins syndrome is found in 1 in 10,000 births. The typical physical features include downward slanting eyes, micrognathia (a small lower jaw), conductive hearing loss, underdeveloped zygoma, drooping part of the lateral lower eyelids, and malformed or absent ears.

Symptoms:
Treacher-Collins syndrome is caused by a defective protein called treacle. The condition is passed down through families (inherited). More than half of all cases are thought to be due to new gene changes (mutations) because there is no family history of the disease.

This condition may vary in severity from generation to generation and from person to person.

Outer part of the ears are abnormal or almost completely missing
Hearing loss
Very small jaw (micrognathia)
Very large mouth
Defect in the lower eyelid (coloboma)
Scalp hair that reaches to the cheeks
Cleft palate

Stem Cell Therapy:
Now, such incurable diseases can be treated by Stem Cell Therapy.

Where Stem cells are being taken from patient’s own bone marrow, Adipose derived fat stem cells, peripheral blood derived stem cells or Umbilical cord blood-derived & placenta-derived immune rejection free stem cells. No. of experts in different parts of the world say Germany, Mexico, Ukraine, India, China and many more have treated thousands of patients suffering from incurable disease improving their Life quality.

To get your medical condition evaluated by this global medical experts team & to contact experienced patients in this regard, contact SCGF or become its member.

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