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- W2206979551 abstract "Introduction: Pseudohypoparathyroidism (PHPT) is characterized with end-organ resistance to parathormone (PTH) although normal hormone secretion and divided into two groups as Type 1 and Type 2. Furthermore, Type 1 PHPT is subdivided into 3 subgroups as ‘a’, ‘b’ and ‘c’. Case: Ten years old male case has admitted to our department with numbness and spasm in hands and we have detected hypocalcemia, hyperphosphatemia and increased parathormone levels. Cranial computed tomography revealed patchy calsific areas in phenotypically normal case. Conclusion: We primarily considered the case as having PHPT Type 1b or Type 2 and started active vitamine D and calcium replacement therapies which improved clinical and laboratory findings." @default.
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- W2206979551 date "2014-01-01" @default.
- W2206979551 modified "2023-09-29" @default.
- W2206979551 title "A pseudohypoparathyroidism case with rarely seen intracranial calcification in childhood" @default.
- W2206979551 doi "https://doi.org/10.5222/buchd.2014.214" @default.
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