Restriction of lung volumes but normal function of pulmonary tissue in mulibrey nanism

Background Mulibrey nanism (MUL) is a rare growth restriction disorder with multiple organ manifestations caused by genetic defects affecting the TRIM37 protein. A perimyocardial heart disease is the most serious manifestation. Many MUL children appear to suffer from airway obstruction related to in...

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Veröffentlicht in:Pediatric pulmonology 2020-01, Vol.55 (1), p.122-129
Hauptverfasser: Sivunen, Johanna, Piirilä, Päivi, Karlberg, Susann, Kajosaari, Merja, Valmari, Pekka, Kupari, Markku, Lipsanen‐Nyman, Marita, Jalanko, Hannu, Sovijärvi, Anssi RA
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Sprache:eng
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Zusammenfassung:Background Mulibrey nanism (MUL) is a rare growth restriction disorder with multiple organ manifestations caused by genetic defects affecting the TRIM37 protein. A perimyocardial heart disease is the most serious manifestation. Many MUL children appear to suffer from airway obstruction related to infection or exercise, prompting use of inhaled therapies. Asthma medication is continued up to adolescence or even to adulthood due to persisting of symptoms. The pulmonary pathophysiology has previously not been evaluated in any MUL cohort. Methods Thirty three finnish MUL patients (median age 20 years) were investigated with several lung function tests: spirometry with bronchodilatation test, single‐breath diffusing capacity for carbon monoxide, single‐breath lung volume measurements with helium dilution, and thoracic gas volume, airway resistance and specific conductance measurements with a body plethysmograph. As MUL typically affects body proportions, all variables were compared with reference values and with predicted values calculated from sitting height. Results Total lung capacity and forced vital capacity were markedly reduced (total lung capacity [TLC] and forced vital capacity [FVC], P 
ISSN:8755-6863
1099-0496
DOI:10.1002/ppul.24518