Osteoma cutis in Albright's Hereditary Osteodystrophy / 대한피부과학회지
Korean Journal of Dermatology
;
: 493-495, 2004.
Article
in Korean
| WPRIM
| ID: wpr-159986
ABSTRACT
Albright's hereditary osteodystrophy is an inherited syndrome that encompasses endocrinologic anomaly of pseudohypoparathyroidim or less commonly, pseudo-pseudohypoparathyroidism and various physical stigmata such as mental retardation, short stature, skeletal anomaly of the hands, abnormal dentition, round facies, and osteoma cutis. Primary osteoma cutis in this syndrome presents at birth or in early infancy, preceding most of the other manifestations. This case is a typical presentation with osteoma cutis as the sole initial manifestation. Rather unfamiliar to dermatologists, Albright's hereditary osteodystrophy still deserves to be included in the differentials when an isolated case of osteoma cutis presents in a young child.
Full text:
Available
Index:
WPRIM (Western Pacific)
Main subject:
Osteoma
/
Pseudopseudohypoparathyroidism
/
Christianity
/
Facies
/
Parturition
/
Dentition
/
Hand
/
Intellectual Disability
Limits:
Child
/
Humans
Language:
Korean
Journal:
Korean Journal of Dermatology
Year:
2004
Type:
Article
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