X-Linked Hypophosphatemia: A “Family Diagnosis”
X-linked hypophosphatemia can remain undiagnosed across generations when symptoms are mistaken for normal childhood development or ordinary family traits. Here, we look at diagnostic barriers, the importance of testing and genetic counseling, and how identifying one patient can prompt a cascade of family diagnoses. When Emily’s seven-month-old daughter Ila began pulling herself up to stand, […]
The post X-Linked Hypophosphatemia: A “Family Diagnosis” appeared first on Endocrine News.
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