A cephalometric study of patients with cystic fibrosis

Children with cystic fibrosis have skeletal maturation and epiphyseal anomalies similar to those in children with nutritional problems. However, these patients have been found to have normal somatic development if treatment is begun early. In a group of children with cystic fibrosis undergoing medic...

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Podrobná bibliografia
Vydané v:The Journal of the American Dental Association (1939) Ročník 96; číslo 1; s. 83
Hlavní autori: Reitman, A A, Faber, R D
Médium: Journal Article
Jazyk:English
Vydavateľské údaje: England 01.01.1978
Predmet:
Adolescent
Adult
Cephalometry
Child
Child, Preschool
Cystic Fibrosis
Female
Humans
Male
Maxillofacial Development
Skull - growth & development
ISSN:0002-8177
On-line prístup:Zistit podrobnosti o prístupe
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Popis
Shrnutí:Children with cystic fibrosis have skeletal maturation and epiphyseal anomalies similar to those in children with nutritional problems. However, these patients have been found to have normal somatic development if treatment is begun early. In a group of children with cystic fibrosis undergoing medical treatment, cephalometric measurements compared favorably with those established by normal standards.
Bibliografia:ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-1
content type line 23
ISSN:0002-8177
DOI:10.14219/jada.archive.1978.0001