AI Article Synopsis

  • ABCA3 protein deficiency due to gene mutations is primarily linked to respiratory distress in newborns and, less commonly, in adults with interstitial lung diseases (ILD).
  • A specific adult patient with two genetic mutations, including a likely pathogenic one, experienced a worsening condition of late-onset fibrotic ILD despite corticosteroid treatments.
  • Following treatment with hydroxychloroquine, the patient's condition rapidly improved and remained stable for over 6.5 years, enabling removal from the lung transplant list.

Article Abstract

The gene mutations responsible for ABCA3 protein deficiency are involved in respiratory distress of the newborn and much more rarely in adult interstitial lung diseases (ILD). An adult patient homozygous for a complex allele encompassing the p.Ala1027Pro likely pathogenic mutation and the p.Gly974Asp variation was followed for a late-onset and fibrotic ILD. The evolution was marked by progressive clinical and functional degradation despite corticosteroid pulses. The patient, who was first registered on the list for lung transplantation, was improved quickly and persistently for at least 6.5 years with hydroxychloroquine treatment, allowing removal from the transplant list.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9437752PMC
http://dx.doi.org/10.36141/svdld.v39i2.12730DOI Listing

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