Matilda Hatton has Sensenbrenner Syndrome, which causes her to have morphic facial features and shorter limbs. Matilda Hatton's syndrome is so rare it took doctors three years to work out what she ...

Dutch researchers have found a new gene for Sensenbrenner syndrome. The mutation adds support to the hypothesis that defects in ciliar transport are the cause of the disease. Dutch researchers of ...

Matilda Hatton, aged seven, from Walsall, has Sensenbrenner Syndrome. The disease means she has morphic facial features, shorter limbs and grows at a slower rate than other children. She was born ...

Matilda Hatton suffers from Sensenbrenner Syndrome which causes her to have morphic facial features and shorter limbs. The youngster grows at a slower rate than other children because of the ...

Matilda Hatton, aged seven, from Walsall, has Sensenbrenner Syndrome, but she wasn’t diagnosed until she was three years old because doctors were baffled by her symptoms. The disease means she ...

Matilda Hatton, aged seven, has Sensenbrenner Syndrome, which means she has morphic facial features, shorter limbs and grows at a slower rate than other children. Little is known about the condition.

Matilda Hatton, aged seven, from Walsall, has Sensenbrenner Syndrome. The disease means she has morphic facial features, shorter limbs and grows at a slower rate than other children. She was born ...