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An ICF Core Set can serve as a reference framework and a practical tool to classify and describe patient functioning in a more time efficient way. ICF Core Sets can be used along the continuum of care and over the course of a health condition. [10] The ICF classification includes more than 1,400 categories limiting its use in clinical practice ...
ICF syndrome patients exhibit facial anomalies which include hypertelorism, low-set ears, epicanthal folds and macroglossia. [3] Other frequent symptoms observed in individuals with ICF syndrome include intellectual disability, recurrent and prolonged respiratory infections, and integumentary and digestive system infections.
The WHO-FIC contains three Reference Classifications: the ICD-11 MMS (see below), the ICF, and the ICHI. Derived Classifications are based on the three Reference Classifications, and are usually tailored for a particular specialty. [20] For example, the ICD-O is a Derived Classification used in oncology. Each node of the Foundation has a unique ...
Archives of Disease in Childhood is a peer-reviewed medical journal published by the BMJ Group and covering the field of paediatrics. It is the official journal of the Royal College of Paediatrics and Child Health. [1]
Paediatrics & Child Health is a peer-reviewed medical journal of paediatrics [1] and is the official journal of the Canadian Paediatric Society. [1] It covers original research, practice guidelines, and continuing medical education. The journal was originally published by the Pulsus Group, but was transferred to Oxford University Press in 2016 ...
Clinical Pediatrics is abstracted and indexed in, among other databases: SCOPUS, and the Social Sciences Citation Index. According to the Journal Citation Reports, its 2018 impact factor is 1.383, ranking it 78 out of 125 journals in the category 'Pediatrics'. [1]
The journal was conceived as a general pediatrics journal and its original aim was to "give studies from the Nordic countries a worldwide audience." [ 1 ] Thus the journal was originally trilingual, publishing papers in English, German, and French, at a time when most medical journals were still published in national languages; the journal ...
Severe combined immunodeficiency (SCID), also known as Swiss-type agammaglobulinemia, is a rare genetic disorder characterized by the disturbed development of functional T cells and B cells caused by numerous genetic mutations that result in differing clinical presentations. [2]