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Osteoma cutis in pseudohypoparathyroidism.
Dermatology 1999; 198(2):209-11D

Abstract

Pseudohypoparathyroidism (PHP) is a hereditary disorder characterized by an end-organ resistance for parathormone. PHP can be classified into different types by biochemical and phenotypic characteristics and the level of the defect in the hormone-receptor complex. PHP is described as Albright's hereditary osteodystrophy (AHO) when a specific phenotype is present. We report a case of osteoma cutis in a 30-year-old woman with AHO. Successful treatment was obtained by debriding the lesion followed by split-thickness skin grafting.

Authors+Show Affiliations

Department of Dermatology, University Hospital Gent, Belgium.No affiliation info availableNo affiliation info available

Pub Type(s)

Case Reports
Journal Article

Language

eng

PubMed ID

10325484

Citation

Goeteyn, V, et al. "Osteoma Cutis in Pseudohypoparathyroidism." Dermatology (Basel, Switzerland), vol. 198, no. 2, 1999, pp. 209-11.
Goeteyn V, De Potter CR, Naeyaert JM. Osteoma cutis in pseudohypoparathyroidism. Dermatology (Basel). 1999;198(2):209-11.
Goeteyn, V., De Potter, C. R., & Naeyaert, J. M. (1999). Osteoma cutis in pseudohypoparathyroidism. Dermatology (Basel, Switzerland), 198(2), pp. 209-11.
Goeteyn V, De Potter CR, Naeyaert JM. Osteoma Cutis in Pseudohypoparathyroidism. Dermatology (Basel). 1999;198(2):209-11. PubMed PMID: 10325484.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Osteoma cutis in pseudohypoparathyroidism. AU - Goeteyn,V, AU - De Potter,C R, AU - Naeyaert,J M, PY - 1999/5/15/pubmed PY - 2000/8/16/medline PY - 1999/5/15/entrez SP - 209 EP - 11 JF - Dermatology (Basel, Switzerland) JO - Dermatology (Basel) VL - 198 IS - 2 N2 - Pseudohypoparathyroidism (PHP) is a hereditary disorder characterized by an end-organ resistance for parathormone. PHP can be classified into different types by biochemical and phenotypic characteristics and the level of the defect in the hormone-receptor complex. PHP is described as Albright's hereditary osteodystrophy (AHO) when a specific phenotype is present. We report a case of osteoma cutis in a 30-year-old woman with AHO. Successful treatment was obtained by debriding the lesion followed by split-thickness skin grafting. SN - 1018-8665 UR - https://www.unboundmedicine.com/medline/citation/10325484/Osteoma_cutis_in_pseudohypoparathyroidism_ L2 - https://www.karger.com?DOI=10.1159/000018115 DB - PRIME DP - Unbound Medicine ER -