FAHR'S SYNDROME IN A PATIENT WITH PSEUDOHYPOPARATHYROIDISM – AN INTERESTING CASE REPORT
Author:
Affiliation:
1. Postgraduate Student, Postgraduate Department of Medicine, S.C.B Medical College & Hospital, Cuttack
2. Assistant Professor, Postgraduate Department of Medicine, S.C.B. Medical College & Hospital, Cuttack.
Abstract
Publisher
World Wide Journals
Reference10 articles.
1. Shafiq S, Hafir MA, Maheen et al. Fahr’s syndrome: Literature review of current evidence. Orphanet J Rare Dis 2013;8:156.
2. Yamada N, Hayashi T. Asymptomatic familial basal ganglia calcification with autosomal dominant inheritance: a family report. No Tpo Hattatsu 2000 Nov;32(6):515-9.
3. Geschwind DH, Loginov M, Stern JM. Identification of a locus on chromosome 14q for idiopathic basal ganglia calcification (Fahr disease). Am J Hum Genet. 1999;65(3):764-772.
4. Manyam BV, Walters AS, Narla KR. Bilateral striopallidodendate calcinosis: Clinical characteristics of patients seen in a registry. Mov Disord. 2001;16(2):258-64.
5. Ucciferro P, Anastasopoulou C. Psuedohypoparathyroidism. [Updated 2020 Aug 10]. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing;2021 Jan.
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