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Neumol Pediatr 2016; 11 (1): 15 - 18

Test de sudor en rango intermedio: desafío diagnóstico

REFERENCIAS

1.

Paranjupe S, Zeitlin P. Atypical Cystic Fibrosis and CFTR-

Related Diseases. Clinic Rev Allerg Immunol 2008; 35:116-

123

2.

Grupo Técnico, Programa de Fibrosis Quística Unidad de

Salud Respiratoria , Subsecretaría de Redes Asistenciales

Ministerio de Salud, Programa Nacional de Fibrosis Quística

Orientaciones Técnicas Programáticas para Diagnóstico y

Tratamiento. 2012

3.

Bombieri C, Claustres M, De Boeck K, Derichs N, Dodge J,

Girodon

E.et

al . Recommendations for the classification of

diseases as CFTR-related disorders. Cyst Fibros 2011; 10

suppl 2: s86-s102

4.

Bush A. Diagnóstico de fibrosis quística. Lo fácil, lo difícil, lo

imposible. Neumol Pediatr 2010; 5: 15-22

5.

Farrell P, Rosenstein B, White T, Accurso F, Castellani C,

Cutting G et al. Guidelines for Diagnosis of Cystic Fibrosis in

Newborns Through Older Adults: Cystic Fibrosis Foundation

Consensus Report. J Pediatr 2008 ; 153:s4-s14

6.

Schram C. Atypical Cystic Fibrosis . Identification in the

primary care setting. Can Fam Physician 2012 ;58:1341-

1345

7.

Levy H, Farrell P. New Challenges in the Diagnosis and

Management of Cystic Fibrosis. J Pediatr 2015; 166:1337-

1340

8.

Groves T, Robinson P, Willey V, Fitzgerald D. Long Term

Outcomes of Children with Intermediate Sweat Chloride

Values in Infancy. J Pediatr 2015;166:1469-1474

9.

Massie J. Clements B and the Australian Paediatric

Respiratory Group. Diagnosis of Cystic Fibrosis After

Newborn Screening: The Australasian Experience-Twenty

Years and Five Million Babies Later: A Consensus Statement

From the Australasian Paediatric Group. Pediatr Pulmonol

2005; 39: 440-446

10. Goubau C, Wilschanski, Skalincka V, Lebecque P, Southern

K, Sermet I et al. Phenotypic characterization of patients

with intermediate sweat chloride values: towards validation

of the European diagnostic algorithm for cystic fibrosis.

Thorax 2009; 64: 683-691

11. Ren C, Desai H, Platt M, Dixon M. Clinical Outcomes in

Infants With CysticFibrosis Transmebrane Regulator (CFTR)

Related Metabolic Syndrome. Pediatr Pulmonol 2011; 46:

1079-1084

12. Borowitz D, Parad R, Sharp J, Sabadosa K, Robinson K, Rock

M et al. Cystic Fibrosis Foundation Practice Guidelines for the

Management of Infants with Cystic Fibrosis Transmembrane

Conductance Regulator-Related Metabolic Syndrome during

the First Two Years of Life and Beyond. J Pediatr 2009; 155:

s 106-s116

13. Mayell S, Munck A, Craig J, Sermet I, Brownlee K, Schwarz

M, Castellani C, Southern K. A European consensus for the

evaluation and management of infants with an equivocal

diagnosis following newborn screening for cystic fibrosis. J

Cyst Fibros 2009;8:71-78

14. Brodlie M, Haq IJ , Roberts K , Elborn JS. Targeted therapies

to improve CFTR function in cystic fibrosis. Gen Med 2015;

7:101-116

15. Temme R, Roggenbuck J, McNamara J. CF versus CRMS

:Diagnostic Challenges in Cystic Fibrosis. Minn Med2012;

10 : 42-44

16. Megan N, Adamski C, Tluczeck A. Clinical practices for

intermediate sweat tests following abnormal cystic fibrosis

newborn screens. J Cyst Fibros 2011; 10: 460-465

17. Parra G, Bozzo R, Palomino MA. Fibrosis quística y enfermedad

del CFTR: a propósito de un caso de traqueobroncopatía

osteocondroplástica. Neumol Pediatr 2016;11:45-49