An odd precocious case of progressive osseous heteroplasia

2021 ◽  
Vol 156 (3) ◽  
Author(s):  
Carmelo SCHEPIS ◽  
Maria LENTINI ◽  
Francesco CALÌ
Keyword(s):  
Progressive Osseous Heteroplasia

Progressive osseous heteroplasia

1996 ◽  
Vol 132 (7) ◽  
pp. 787-791 ◽  
Author(s):  
E. S. Miller
Keyword(s):  
Progressive Osseous Heteroplasia

Progressive osseous heteroplasia in a Chinese infant and a novel mutation in the GNAS gene

2017 ◽  
Vol 32 (6) ◽  
pp. e209-e211
Author(s):  
S.-D. Zhang ◽  
Z.-l. Xie ◽  
K.-Q. Zhang ◽  
K. NH-Tseung ◽  
J.-J. Zhao
Keyword(s):  
Novel Mutation ◽  
Gnas Gene ◽  
Progressive Osseous Heteroplasia

Progressive osseous heteroplasia

1994 ◽  
Vol 76 (3) ◽  
pp. 425-436 ◽  
Author(s):  
F S Kaplan ◽  
R Craver ◽  
G D MacEwen ◽  
F H Gannon ◽  
G Finkel ◽  
...  
Keyword(s):  
Progressive Osseous Heteroplasia

scholarly journals Unilateral progressive osseous heteroplasia

2009 ◽  
Vol 19 (3) ◽  
pp. 214-215
Author(s):  
Felicidade Santiago ◽  
Ricardo Vieira ◽  
Margarida Cordeiro ◽  
Óscar Tellechea ◽  
Américo Figueiredo
Keyword(s):  
Progressive Osseous Heteroplasia

Progressive osseous heteroplasia, as an isolated entity or overlapping with Albright hereditary osteodystrophy

2015 ◽  
Vol 28 (7-8) ◽  
Author(s):  
Maria H. Lin ◽  
Nawaporn Numbenjapon ◽  
Emily L. Germain-Lee ◽  
Pisit Pitukcheewanont
Keyword(s):  
Lower Extremity ◽  
Ct Scan ◽  
Wide Spectrum ◽  
Subcutaneous Tissue ◽  
Muscle Pathology ◽  
Limited Joint Mobility ◽  
Albright Hereditary Osteodystrophy ◽  
Genomic Study ◽  
Vitamin D Levels ◽  
Progressive Osseous Heteroplasia

AbstractProgressive osseous heteroplasia (POH) is a condition of invasive heterotopic ossification. Reports of patients with mild POH with Albright hereditary osteodystrophy (AHO), specifically pseudohypoparathyroidism type Ia (PHP Ia) with hormonal resistance, suggest the possibility of a common molecular basis.A 4-year-old boy with obesity, speech delay, and expanding subcutaneous masses on buttock/forearm. Physical exam revealed round facies and brachydactyly. Blood tests showed normal Ca, P, Mg, 25-OH vitamin D levels but elevated parathyroid hormone (PTH) and thyroid-stimulating hormone (TSH). Abdominal computed tomography (CT) showed areas with calcifications in the subcutaneous tissue, fat, and muscle. Pathology of excised tissue revealed ossifications. Genomic study revealed noA 3-year-old boy with painful ossifications in the left lower extremity. Lab tests were notable for elevated PTH and high-normal TSH. The CT-scan showed subcutaneous/intramuscular calcifications. Genetic testing showedA 9-year-old boy with knee pain and subcutaneous ossifications in back and upper/lower extremity, causing significantly limited joint mobility. Lab tests were normal. The CT-scan showed areas corresponding to subcutaneous/intramuscular ossifications throughout torso and extremities, consistent with POH. There was noPatients with heterotopic ossifications present with a wide spectrum of disease. Although

Progressive Osseous Heteroplasia. A Case Report and Review of the Literature

2002 ◽  
Vol 11 (4) ◽  
pp. 339-342
Author(s):  
Osman Aynaci ◽  
F. Müjgan Aynaci ◽  
Ümit Çobanoğlu ◽  
Köksal Alpay
Keyword(s):  
Case Report ◽  
Review Of The Literature ◽  
Progressive Osseous Heteroplasia

Progressive osseous heteroplasia resulting from a new mutation in the GNAS1 gene

2004 ◽  
Vol 29 (1) ◽  
pp. 77-80 ◽  
Author(s):  
I. Chan ◽  
T. Hamada ◽  
C. Hardman ◽  
J. A. McGrath ◽  
F. J. Child
Keyword(s):  
New Mutation ◽  
Gnas1 Gene ◽  
Progressive Osseous Heteroplasia
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