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Chondrocalcinosis related to familial hypomagnesemia with hypercalciuria and nephrocalcinosis

Journal of Pediatric Endocrinology and Metabolism · Mayıs 2015

Özet
Calcium pyrophosphate dehydrate (CPPD) crystal deposition disease (also known as chondrocalcinosis, CC) is a rare metabolic arthropathy mostly seen in elderly patients. Chondrocalcinosis may be associated with metabolic diseases such as hypomagnesemia when it occurs in young people. We report here a case with hypomagnesemia due to familial hypomagnesemia with hypercalciuria and nephrocalcinosis (FHHNC) who developed CC during clinical follow-up. To our best knowledge this is the first case of a young patient with CPPD associated with FHHNC.
6 atıf Mayıs 2015 DOI
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YÖKSİS Kayıtları
Chondrocalcinosis related to familial hypomagnesemia with hypercalciuria and nephrocalcinosis
Journal of Pediatric Endocrinology and Metabolism · 2015 SCI-Expanded
Prof. Dr. HARUN PERU →
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Makale Bilgileri

Toplam Atıf 6 atıf · Scopus
ISSN0334018X
Yayın TarihiMayıs 2015
Cilt / Sayfa28 · 713-716

Kurumlar

Selçuk Üniversitesi
Selçuklu Turkey

Havuzumuzdaki Atıflar 0

Bu makaleye, sistemimizdeki Scopus veritabanında bulunan 0 makale atıf yapmıştır. Scopus genel atıf sayısı: 6.

Bu makaleye, kendi Scopus havuzumuzdaki başka bir makaleden atıf kaydı bulunmuyor.
Scimago Dergi (ISSN Eşleşmesi)
Journal of Pediatric Endocrinology and Metabolism
Q3
SJR Skoru0,363
H-Index76
YayıncıWalter de Gruyter GmbH
ÜlkeGermany
Endocrinology, Diabetes and Metabolism (Q3)
Pediatrics, Perinatology and Child Health (Q3)
Endocrinology (Q4)
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6
Atıf

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