An Interactive Annotated World Bibliography of Printed and Digital Works in the History of Medicine and the Life Sciences from Circa 2000 BCE to 2024 by Fielding H. Garrison (1870-1935), Leslie T. Morton (1907-2004), and Jeremy M. Norman (1945- ) Traditionally Known as “Garrison-Morton”

16061 entries, 14144 authors and 1947 subjects. Updated: December 10, 2024

Permanent Link for Entry #5989

  • 4395.1

Ein Fall von Osteopathia hyperostotica (sclerotisans) multiplex infantilis.

Fortschr. Röntgenstr., 39, 1101-06, 1929.

“Engelmann’s disease”,  also known as "Camurati-Engelmann disease" — a very rare autosomal dominant genetic disorder that causes characteristic anomalies in the skeleton. It is a form of dysplasia, causing osteosclerosis. See No. 7832.



Subjects: GENETICS / HEREDITY › HEREDITARY / CONGENITAL DISEASES OR DISORDERS › Hereditary Disorders of the Skeleton, ORTHOPEDICS › Diseases of or Injuries to Bones, Joints & Skeleton › Congenital Diseases
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