Results 251 to 260 of about 84,871 (291)
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TIPS IN DIAGNOSING FETAL SKELETAL ANOMALIES
Obstetrics and Gynecology Clinics of North America, 1998A systematic approach to the prenatal and postnatal evaluation of the patient at risk for fetal skeletal anomalies is outlined. The more common anomalies are described within a differential diagnosis table, and a case study is presented.
O A, Rust, K G, Perry, W E, Roberts
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Canadian Journal of Animal Science, 1963
Skeletal anomalies, principally of the axial skeleton, occurred with a frequency of 0.28 per cent in a population of 10,683 pigs produced over an 8-year period. These anomalies are described and possible genetic interpretations considered. It was concluded that they were manifestations of metabolic disturbances of non-genetic origin occurring at ...
H. T. Fredeen, Leon Jarmoluk
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Skeletal anomalies, principally of the axial skeleton, occurred with a frequency of 0.28 per cent in a population of 10,683 pigs produced over an 8-year period. These anomalies are described and possible genetic interpretations considered. It was concluded that they were manifestations of metabolic disturbances of non-genetic origin occurring at ...
H. T. Fredeen, Leon Jarmoluk
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Skeletal Anomalies Associated with Unilateral Renal Agenesis
British Journal of Urology, 1987Summary— Unilateral renal agenesis is sometimes associated with skeletal anomalies. The skeletal malformations are easily detectable and, if found, should suggest further urological investigations. The embryological aspect of the association is explored.
N P, Gupta, I B, Gill
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Multiple skeletal anomalies in the ?13q-? syndrome
European Journal of Pediatrics, 1978A patient with the "13q-" syndrome is reported. The typical association of congenital malformations was found. Multiple and unusual skeletal anomalies included absent thumbs, club-feet, coxa vara, diastasis of the pubic symphisis and extensive spina bifida occulta.
J, Chemke +3 more
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Common congenital skeletal anomalies of the thorax
Journal of Thoracic Imaging, 1986Bony anomalies of the thorax may occur as isolated problems, but are also seen in conjunction with other skeletal or organ anomalies. Among the most common thoracic osseous anomalies are pectus excavatum, pectus carinatum, sternal ossification abnormalities, and deformity of the spine, ribs, clavicle, or scapula.
H T, Harcke +3 more
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Cloverleaf skull associated with unusual skeletal anomalies
Pediatric Radiology, 1987A male infant with cloverleaf skull and multiple other birth defects born to unrelated, healthy, young parents is presented. Radiologic findings in addition to the cloverleaf skull configuration included short, wide clavicles, winged scapulae, unusual shapes of ribs with abnormal spacing between them and with prominent costovertebral junctions, and ...
B, Say, A K, Poznanski
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Cutis Laxa, Skeletal Anomalies, and Ambiguous Genitalia
Archives of Pediatrics & Adolescent Medicine, 1974A patient exhibited cutis laxa, short digits, absent phalanges, and ambiguous genitalia. There is a relationship between serum levels of copper, elastase inhibitor, and α 1 -antitrypsin to cutis laxa.
C I, Kaye, D E, Fisher, N B, Esterly
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Phenotypic progression of skeletal anomalies in CLOVES syndrome
American Journal of Medical Genetics Part A, 2012AbstractOvergrowth syndromes, defined as genetic disorders in which there is disproportionate somatic growth, are challenging to diagnose due to their heterogeneous presentations and possible differing genetic etiologies. CLOVES syndrome is characterized by congenital lipomatous overgrowth, vascular malformations, epidermal nevi, and skeletal ...
Steven, Klein +3 more
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Relationship between transverse dental anomalies and skeletal asymmetry
American Journal of Orthodontics and Dentofacial Orthopedics, 2003The recognition and elimination of dental compensation is essential in presurgical orthodontic treatment to achieve successful stabilization of the occlusion after surgery. However, the relationship between a transverse dental anomaly and skeletal asymmetry is not fully understood.
Masaomi, Kusayama +2 more
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Fibrodysplasia ossificans progressiva without characteristic skeletal anomalies
Rheumatology International, 2010Fibrodysplasia ossificans progressiva (FOP) is a rare but extremely disabling genetic disease of the skeletal system. This disease is characterized by progression of heterotopic ossification within skeletal muscles, ligaments and tendons. Most patients with FOP are misdiagnosed early in life before the appearance of heterotopic ossification and undergo
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