Pseudohypoparathyroidism with Albright hereditary osteodystrophy (Q90506): Difference between revisions
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A osteodistrofia hereditária de Albright é uma síndrome com uma ampla gama de manifestações, incluindo baixa estatura, obesidade, face arredondada, ossificações subcutâneas e encurtamento e alargamento característicos dos ossos longos das mãos e pés (braquidactilia afetando principalmente os 4º e 5º metacarpos). Essas características somáticas estão associadas ao pseudo-hipoparatireoidismo tipo 1a ou 1c e ao pseudopseudo-hipoparatireoidismo. | |||
| description / en | description / en | ||
Albright hereditary osteodystrophy (AHO) is a syndrome with a wide range of manifestations including short stature, obesity, rounded face, subcutaneous ossifications and characteristic shortening and widening of long bones in the hands and feet (brachydactyly mostly affecting the 4th and 5th rays). These somatic features are associated with pseudohypoparathyroidism type 1a or 1c and to pseudopseudohypoparathyroidism. | |||
Revision as of 17:29, 15 August 2026
Albright hereditary osteodystrophy (AHO) is a syndrome with a wide range of manifestations including short stature, obesity, rounded face, subcutaneous ossifications and characteristic shortening and widening of long bones in the hands and feet (brachydactyly mostly affecting the 4th and 5th rays). These somatic features are associated with pseudohypoparathyroidism type 1a or 1c and to pseudopseudohypoparathyroidism.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1271422188 |
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| English | Pseudohypoparathyroidism with Albright hereditary osteodystrophy |
Albright hereditary osteodystrophy (AHO) is a syndrome with a wide range of manifestations including short stature, obesity, rounded face, subcutaneous ossifications and characteristic shortening and widening of long bones in the hands and feet (brachydactyly mostly affecting the 4th and 5th rays). These somatic features are associated with pseudohypoparathyroidism type 1a or 1c and to pseudopseudohypoparathyroidism. |
