- Caffey syndrome
- Caffey-Silverman syndrome infantile cortical hyperostosis.
Medical dictionary. 2011.
Caffey syndrome
Look at other dictionaries:
Caffey syndrome — ▪ pathology also called infantile cortical hyperostosis a hereditary disease of infants, characterized by swellings of the periosteum (the bone layer where new bone is produced) and the bone cortex of the upper arms, shoulder girdle, and… … Universalium
Kenny-Caffey syndrome — Ken·ny Caf·fey syndrome (kenґe kafґe) [Frederic Marshal Kenny, American pediatrician, born 1929; John Patrick Caffey, American pediatrician, 1895–1978] see under syndrome … Medical dictionary
Kenny-Caffey syndrome — a hereditary syndrome characterized by hypoparathyroidism with intermittent hypocalcemia, short stature, and medullary stenosis of tubular bones. It is usually autosomal dominant, but autosomal recessive cases have also been observed … Medical dictionary
syndrome — The aggregate of symptoms and signs associated with any morbid process, and constituting together the picture of the disease. SEE ALSO: disease. [G. s., a running together, tumultuous concourse; (in med.) a concurrence of symptoms, fr. syn,… … Medical dictionary
Caffey — John Patrick, U.S. physician, radiologist, and pediatrician, the “the father of pediatric radiology”, 1895–1978. See C. disease, C. syndrome, C. Kempe syndrome, C. Silverman syndrome … Medical dictionary
Shaken baby syndrome — Classification and external resources ICD 9 995.55 MedlinePlus 000004 … Wikipedia
Charlotte Caffey — (2008) Background information Birth name Charlotte Irene Caffey … Wikipedia
síndrome de Caffey — Eng. Caffey s syndrome Síndrome de etiología desconocida que se manifiesta en los primeros meses de vida como una tumefacción de partes blandas e hiperostosis cortical extensa. A nivel oftalmológico las principales manifestaciones son edema… … Diccionario de oftalmología
síndrome de Caffey-Silverman — Eng. Caffey Silverman syndrome Ver síndrome de Caffey … Diccionario de oftalmología
Liste Des Maladies Génétiques À Gène Identifié — Ceci est la liste des maladies génétiques à gène identifié. Voir aussi la : liste des maladies génétiques à gène non identifié. Les maladies génétiques citées ici sont les maladies génétiques dont le gène est connu (Symbole + de MIM) ou dont … Wikipédia en Français
