Pfeiffer-Hirschfelder-Rott syndrome: A very rare syndrome characterized by facial and kidney anomalies and a type of dwarfism where the farthest parts of the limbs suffer the greatest degree of shortness. More detailed information about the symptoms, causes, and treatments of Pfeiffer-Hirschfelder-Rott syndrome is available below.
See full list of 11 symptoms of Pfeiffer-Hirschfelder-Rott syndrome
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Read more about causes of Pfeiffer-Hirschfelder-Rott syndrome.
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Read more about Misdiagnosis and Pfeiffer-Hirschfelder-Rott syndrome
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Choosing the Best Hospital: More general information, not necessarily in relation to Pfeiffer-Hirschfelder-Rott syndrome, on hospital performance and surgical care quality:
Types of Pfeiffer-Hirschfelder-Rott syndrome
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Pfeiffer-Hirschfelder-Rott syndrome is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Pfeiffer-Hirschfelder-Rott syndrome, or a subtype of Pfeiffer-Hirschfelder-Rott syndrome,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
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