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What else can I help you with?
Is Prince's son alive?
No, Boy Gregory died a week after birth due to Pfeiffer syndrome, a rare defect of the skull.
Is there a cure for Pfeiffer Syndrome?
No, not yet.
What is syndactyly a symptom of?
Syndactyly is a characteristic of Apert syndrome, Poland syndrome, Jarcho-Levin syndrome, oral-facial-digital syndrome, Pfeiffer syndrome, and Edwards syndrome
Is Tourette syndrome rare?
Once thought to be a rare disorder, TS is one of the most common genetic conditions
What other conditions could an infant with syndactyly have?
Syndactyly is a characteristic of Apert syndrome, Poland syndrome, Jarcho-Levin syndrome, oral-facial-digital syndrome, Pfeiffer syndrome, and Edwards syndrome.
How common is hurler syndrome?
Hurler syndrome is a rare genetic disorder with an estimated incidence of about 1 in 100,000 to 1 in 150,000 live births. It is considered a rare disease.
Is Pfeiffer Syndrome life-threatening?
Pfeiffer syndrome is a genetic disorder that affects the development of the skull, hands, and feet. In severe cases, it can lead to complications that may be life-threatening, such as breathing difficulties due to restricted airways or neurological complications. Regular medical monitoring and management are essential to ensure the best possible outcomes for individuals with Pfeiffer syndrome.
How common is morquio syndrome?
Morquio's Syndrome is a rare, usually inherited disease. The chances of getting this autosomal recessive birth defect is 1 in 200,000.
How common is cri du chat syndrome?
Kind of rare.. One in 50,000 babies get it.. So yea:)
How common are mucopolysaccharidoses?
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.
What is the average age of Reye Syndrome patients?
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.
What is Pfieffer syndrome?
Pfeiffer syndrome is a rare genetic disorder characterized by abnormalities in the shape of the head and face, including early fusion of certain skull bones. This can lead to various physical and developmental challenges, such as hearing loss and cognitive impairments. Treatment typically involves a combination of surgical interventions and ongoing medical management to address the specific symptoms and complications associated with the syndrome.
