Tags

Type your tag names separated by a space and hit enter

[Albright's hereditary osteodystrophy: report of three cases].
Arch Argent Pediatr. 2010 Apr; 108(2):e24-7.AA

Abstract

Albright's hereditary osteodystrophy includes an heterogeneous group of genetic diseases, including the pseudohypoparathyroidism type Ia and pseudo-pseudohypoparathyroidism. Features of this disease are: round faces, over-weight, subcutaneous calcifications and brachydactylia. Pseudohypoparathyroidism type Ia is associated with laboratory abnormalities such as hypocalcemia, and hyperphosphatemia due to parathormone resistance. Furthermore, these patients may present peripheral resistance to other hormones, such as gonadotrophins and thyroids. Pseudo-pseudohypoparathyroidism has no peripheral resistance to these hormones. We present three patients evaluated in our hospital with clinical manifestations of Albright's syndrome.

Authors+Show Affiliations

Servicio de Dermatología, Hospital de Pediatría Prof. Dr. Juan P. Garrahan. mariambujan@yahoo.comNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Case Reports
English Abstract
Journal Article

Language

spa

PubMed ID

20467695

Citation

Bujan, María M., et al. "[Albright's Hereditary Osteodystrophy: Report of Three Cases]." Archivos Argentinos De Pediatria, vol. 108, no. 2, 2010, pp. e24-7.
Bujan MM, Cervini AB, Fano V, et al. [Albright's hereditary osteodystrophy: report of three cases]. Arch Argent Pediatr. 2010;108(2):e24-7.
Bujan, M. M., Cervini, A. B., Fano, V., & Pierini, A. M. (2010). [Albright's hereditary osteodystrophy: report of three cases]. Archivos Argentinos De Pediatria, 108(2), e24-7. https://doi.org/10.1590/S0325-00752010000200012
Bujan MM, et al. [Albright's Hereditary Osteodystrophy: Report of Three Cases]. Arch Argent Pediatr. 2010;108(2):e24-7. PubMed PMID: 20467695.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - [Albright's hereditary osteodystrophy: report of three cases]. AU - Bujan,María M, AU - Cervini,Andrea B, AU - Fano,Virginia, AU - Pierini,Adrián M, PY - 2009/06/11/received PY - 2009/11/17/accepted PY - 2010/5/15/entrez PY - 2010/5/15/pubmed PY - 2010/9/2/medline SP - e24 EP - 7 JF - Archivos argentinos de pediatria JO - Arch Argent Pediatr VL - 108 IS - 2 N2 - Albright's hereditary osteodystrophy includes an heterogeneous group of genetic diseases, including the pseudohypoparathyroidism type Ia and pseudo-pseudohypoparathyroidism. Features of this disease are: round faces, over-weight, subcutaneous calcifications and brachydactylia. Pseudohypoparathyroidism type Ia is associated with laboratory abnormalities such as hypocalcemia, and hyperphosphatemia due to parathormone resistance. Furthermore, these patients may present peripheral resistance to other hormones, such as gonadotrophins and thyroids. Pseudo-pseudohypoparathyroidism has no peripheral resistance to these hormones. We present three patients evaluated in our hospital with clinical manifestations of Albright's syndrome. SN - 1668-3501 UR - https://www.unboundmedicine.com/medline/citation/20467695/[Albright's_hereditary_osteodystrophy:_report_of_three_cases]_ L2 - http://www.scielo.org.ar/scielo.php?script=sci_arttext&pid=S0325-00752010000200012&lng=en&nrm=iso&tlng=en DB - PRIME DP - Unbound Medicine ER -
Try the Free App:
Prime PubMed app for iOS iPhone iPad
Prime PubMed app for Android
Prime PubMed is provided
free to individuals by:
Unbound Medicine.