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[Albright's hereditary osteodystrophy I and cataract].
Oftalmologia. 1995 Apr-Jun; 39(2):109-13.O

Abstract

The 26-year-old female patient presented Albright I hereditary osteodystrophy and zonular cataract, chronic tetany, hypothyroidism. The affection started since she was 3 year old. In the same family there are other 7 persons with hereditary osteodystrophy, from which one of the patient's brothers has Albright II syndrome. It is proved that the pseudoparathyroidism and the pseudopseudohypoparathyroidism are two clinical manifestations of the same affection. The cataract from Albright syndrome is determined by disturbances of the phosphocalcium metabolism and must be distinguished by other endocrine and congenital forms of cataract. The deficiency can be explained by a disturbance of renal function in the reabsorption of phosphates.

Authors+Show Affiliations

Secţia de Oftalmologie, Drobeta Tr.-Severin.

Pub Type(s)

Case Reports
English Abstract
Journal Article

Language

rum

PubMed ID

7766587

Citation

Nicu, C. "[Albright's Hereditary Osteodystrophy I and Cataract]." Oftalmologia (Bucharest, Romania : 1990), vol. 39, no. 2, 1995, pp. 109-13.
Nicu C. [Albright's hereditary osteodystrophy I and cataract]. Oftalmologia. 1995;39(2):109-13.
Nicu, C. (1995). [Albright's hereditary osteodystrophy I and cataract]. Oftalmologia (Bucharest, Romania : 1990), 39(2), 109-13.
Nicu C. [Albright's Hereditary Osteodystrophy I and Cataract]. Oftalmologia. 1995 Apr-Jun;39(2):109-13. PubMed PMID: 7766587.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - [Albright's hereditary osteodystrophy I and cataract]. A1 - Nicu,C, PY - 1995/4/1/pubmed PY - 1995/4/1/medline PY - 1995/4/1/entrez SP - 109 EP - 13 JF - Oftalmologia (Bucharest, Romania : 1990) JO - Oftalmologia VL - 39 IS - 2 N2 - The 26-year-old female patient presented Albright I hereditary osteodystrophy and zonular cataract, chronic tetany, hypothyroidism. The affection started since she was 3 year old. In the same family there are other 7 persons with hereditary osteodystrophy, from which one of the patient's brothers has Albright II syndrome. It is proved that the pseudoparathyroidism and the pseudopseudohypoparathyroidism are two clinical manifestations of the same affection. The cataract from Albright syndrome is determined by disturbances of the phosphocalcium metabolism and must be distinguished by other endocrine and congenital forms of cataract. The deficiency can be explained by a disturbance of renal function in the reabsorption of phosphates. SN - 1220-0875 UR - https://www.unboundmedicine.com/medline/citation/7766587/[Albright's_hereditary_osteodystrophy_I_and_cataract]_ L2 - http://www.diseaseinfosearch.org/result/300 DB - PRIME DP - Unbound Medicine ER -
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