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Autosomal Dominant Osteopetrosis
SSRN Electronic Journal, 2022Autosomal dominant osteopetrosis (ADO) is the most common form of osteopetrosis. ADO is characterized by generalized osteosclerosis along with characteristic radiographic features such as a "bone-in-bone" appearance of long bones and sclerosis of the superior and inferior vertebral body endplates.
Polgreen, Lynda E. +2 more
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American Orthoptic Journal, 2013
Osteopetrosis is a rare disease that occurs when a child has an unequal balance between new bone growth and elimination of old bone. Children with this entity are able to make new bone tissue, but are not able to break down and eliminate old bones, which is essential for normal bone growth. These thickened and enlarged bones are very weak.
Patricia F, Jenkins +3 more
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Osteopetrosis is a rare disease that occurs when a child has an unequal balance between new bone growth and elimination of old bone. Children with this entity are able to make new bone tissue, but are not able to break down and eliminate old bones, which is essential for normal bone growth. These thickened and enlarged bones are very weak.
Patricia F, Jenkins +3 more
openaire +2 more sources
Seminars in Musculoskeletal Radiology, 2002
Osteopetrosis is a rare sclerosing inherited dysplasia of bone caused by the deficient function of osteoclasts. At first the disease was divided into the severe infantile recessive and the more benign autosomal dominant types, but clinical differences and progress in genetic understanding have now enabled identification of two distinct autosomal ...
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Osteopetrosis is a rare sclerosing inherited dysplasia of bone caused by the deficient function of osteoclasts. At first the disease was divided into the severe infantile recessive and the more benign autosomal dominant types, but clinical differences and progress in genetic understanding have now enabled identification of two distinct autosomal ...
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Journal of the American Medical Association, 1933
Osteopetrosis is commonly spoken of as "marble bones"; recently it was referred to as "chalky bones." 1 The condition was first described by Albers-Schonberg 2 in 1904, and it is usually referred to by his name. Reviews of cases may be found in articles by Karshner, 3 Davis, 4 and Alexander.
O. B. MAYER, T. A. PITTS
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Osteopetrosis is commonly spoken of as "marble bones"; recently it was referred to as "chalky bones." 1 The condition was first described by Albers-Schonberg 2 in 1904, and it is usually referred to by his name. Reviews of cases may be found in articles by Karshner, 3 Davis, 4 and Alexander.
O. B. MAYER, T. A. PITTS
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Clinical Nuclear Medicine, 1990
A case of a 3 1/2-year-old female with benign osteopetrosis is presented. There was radiographic evidence of previous fetal sclerosis of bone yielding a "bone-within-a-bone" appearance, but on radiophosphate imaging this fetal sclerosis was not hyperactive and could not be differentiated from the normal diaphysis surrounding it.
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A case of a 3 1/2-year-old female with benign osteopetrosis is presented. There was radiographic evidence of previous fetal sclerosis of bone yielding a "bone-within-a-bone" appearance, but on radiophosphate imaging this fetal sclerosis was not hyperactive and could not be differentiated from the normal diaphysis surrounding it.
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Clinical Orthopaedics and Related Research, 1993
Osteopetrosis is an inherited skeletal condition characterized by increased bone radiodensity. There are three clinical groups: infantile-malignant autosomal recessive, fatal within the first few years of life (in the absence of effective therapy); intermediate autosomal recessive, appears during the first decade of life but does not follow a malignant
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Osteopetrosis is an inherited skeletal condition characterized by increased bone radiodensity. There are three clinical groups: infantile-malignant autosomal recessive, fatal within the first few years of life (in the absence of effective therapy); intermediate autosomal recessive, appears during the first decade of life but does not follow a malignant
openaire +2 more sources

