Results 31 to 40 of about 1,444 (153)
Dystrophic calcifications and Raynaud’s phenomenon in an eight-year old girl [PDF]
Srpski Arhiv za Celokupno Lekarstvo, 2014 Introduction. Dystrophic calcifications are the most common subtype of skin calcinosis. Tumorous soft tissue calcium deposits usually contain hydroxyapatite and amorphous calcium phosphate.
Grebeldinger Slobodan P. +5 more
doaj +1 more source
Miosite ossificante progressiva. Stone man.
Acta Médica Portuguesa, 2001 Myositis ossificans progressiva (MOP) is a rare hereditary connective tissue disease, genetically inherited as an autossomal dominant trait with complete penetrance but variable expression.
J E Fonseca +4 more
doaj +1 more source
A CASE OF MYOSITIS OSSIFICANS PROGRESSIVA [PDF]
Journal of the American Medical Association, 1911 The opportunity of recording the history of this patient I owe to the courtesy of Dr. Lucian D. Clark of Toledo, Ohio, who brought her to me for examination December 7, 1907. History. —The patient, F. B., was a girl of 17. There had been no other case o[ill] myositis ossificans in the family.
openaire +1 more source
Clinical Case Reports, Volume 7, Issue 12, Page 2526-2533, December 2019., 2019 Classical homeopathy can be included among the treatment options for congenital heterotopic ossification. Abstract Classical homeopathy can be included among the treatment options for congenital heterotopic ossification.
Dionysios Tsintzas +4 more
wiley +1 more source
Fibrodysplasia Ossificans Progressiva: A Case Report
Journal of Orthopaedic Surgery, 2013 Fibrodysplasia ossificans progressiva or myositis ossificans is a rare disease characterised by bony deposits or the ossification of soft tissues. It transforms skeletal muscles, tendons, ligaments, fascia, and aponeuroses into heterotopic bony deposits ...
Anoop C Dhamangaonkar +2 more
doaj +1 more source
Fibrodysplasia ossificans progressiva: A case report
Asian Journal of Medical Sciences, 2014 Fibrodysplasia ossificans progressiva (FOP) is a genetic disorder with unknown cause. Disease is characterized by heterotopic ossifications of connective tissue and congenital malformations of distal part of extremities.
Sreedhar Vasala
doaj +1 more source
Heterotopic Ossification: A Comprehensive Review
JBMR Plus, Volume 3, Issue 4, April 2019., 2019 ABSTRACT Heterotopic ossification (HO) is a diverse pathologic process, defined as the formation of extraskeletal bone in muscle and soft tissues. HO can be conceptualized as a tissue repair process gone awry and is a common complication of trauma and surgery.
Carolyn Meyers +9 more
wiley +1 more source
Extensive Circumferential Heterotopic Ossification Discovered at the Base of a Loop Ileostomy
Case Reports in Surgery, Volume 2019, Issue 1, 2019., 2019 Heterotopic ossification is a rare phenomenon defined by the formation of bone within nonossifying soft tissues. A rare variant of heterotopic ossification is heterotopic mesenteric ossification (HMO), in which there is involvement of the mesentery and surrounding intra‐abdominal structures.
Ahmad Bosaily +6 more
wiley +1 more source
American Journal of Biological Anthropology, Volume 186, Issue 3, March 2025.ABSTRACT Objectives In bioarchaeology, the concepts of resilience and frailty, and their quantification through indices, have gathered significant attention. This study is the first to apply, evaluate, and compare skeletal frailty indices and aims to trace frailty over time while identifying methodological challenges in their use on a sample ...
Petrosino +7 more
wiley +1 more source
Osteoma Cutis of the Face in CBCT Images
Case Reports in Dentistry, Volume 2017, Issue 1, 2017., 2017 Osteoma cutis (OC) is a rare benign disorder where osseous nodules form in the reticular layer of normal skin. These nodules are formed by the deposition of lamellar bone and are characterized by osteocytes in the core and osteoclasts around the periphery.
Daniah Alhazmi +5 more
wiley +1 more source