no, the odds of a child getting it is 1 in a 100,000
No, Boy Gregory died a week after birth due to Pfeiffer syndrome, a rare defect of the skull.
No, not yet.
Syndactyly is a characteristic of Apert syndrome, Poland syndrome, Jarcho-Levin syndrome, oral-facial-digital syndrome, Pfeiffer syndrome, and Edwards syndrome
From the website (left) it doesn't appear to be.
Once thought to be a rare disorder, TS is one of the most common genetic conditions
Syndactyly is a characteristic of Apert syndrome, Poland syndrome, Jarcho-Levin syndrome, oral-facial-digital syndrome, Pfeiffer syndrome, and Edwards syndrome.
Morquio's Syndrome is a rare, usually inherited disease. The chances of getting this autosomal recessive birth defect is 1 in 200,000.
Kind of rare.. One in 50,000 babies get it.. So yea:)
The MPS syndromes are considered to be rare. Sanfilippo syndrome appears to be the most common MPS with a reported incidence of one in 70,000.
In the United States, the most common age for Reye syndrome is six to eight years. Reye syndrome is extremely rare in individuals over the age of 18.
Wolf-Hirschhorn syndrome is a very rare genetic disorder. The most common symptom is malformation of the facial features and they are short statured and may have malformations of the organs.
He did have a son named Gregory, but he died shortly after his birth from Pfeiffer syndrome. It was one the factors in his decision to seek answers (religious) and causing him to become a Jehovah's Witness.