Digital clubbing without hypoxia for lysinuric protein intolerance.

Autor: Watanabe D; Center for Medical Genetics, Keio University School of Medicine, Tokyo, Japan; Department of Pediatrics, Yamanashi University School of Medicine, Yamanashi, Japan., Tsujioka Y; Department of Radiology, Keio University School of Medicine, Tokyo, Japan., Nakato D; Center for Medical Genetics, Keio University School of Medicine, Tokyo, Japan., Yamada M; Center for Medical Genetics, Keio University School of Medicine, Tokyo, Japan., Suzuki H; Center for Medical Genetics, Keio University School of Medicine, Tokyo, Japan., Ohnishi T; Department of Pediatrics, Keio University School of Medicine, Tokyo, Japan., Tamai N; Department of Pediatrics, Keio University School of Medicine, Tokyo, Japan., Kijima T; Department of Pediatrics, Keio University School of Medicine, Tokyo, Japan., Takenouchi T; Department of Pediatrics, Keio University School of Medicine, Tokyo, Japan., Miya F; Center for Medical Genetics, Keio University School of Medicine, Tokyo, Japan., Narumi S; Department of Pediatrics, Keio University School of Medicine, Tokyo, Japan., Kosaki K; Center for Medical Genetics, Keio University School of Medicine, Tokyo, Japan. Electronic address: kkosaki@keio.jp.
Jazyk: angličtina
Zdroj: European journal of medical genetics [Eur J Med Genet] 2024 Oct; Vol. 71, pp. 104967. Date of Electronic Publication: 2024 Aug 14.
DOI: 10.1016/j.ejmg.2024.104967
Abstrakt: Digital clubbing is characterized by bulbous enlargement of the terminal segments of the fingers. Hypotheses including hypoxia have been proposed for the pathogenesis of digital clubbing, but the exact pathogenesis of digital clubbing is still uncertain. Lysinuric protein intolerance (LPI) is caused by pathogenic variants in SLC7A7 and is often associated with interstitial lung disease. Previously two patients of LPI with digital clubbing but without hypoxia have been reported. It is unclear whether digital clubbing in LPI is secondary to hypoxia or directly related to SLC7A7 deficiency. Here we report a 6-year-old Japanese boy presented with digital clubbing without hypoxia. He had episodic vomiting, each episode consisting of a single vomiting event occurring once a month, and his growth had been delayed. He had interstitial lung disease and hepatomegaly. He had compound heterozygous pathogenic variants in the SLC7A7, leading to the diagnosis of LPI. Together with the two previously reported patients mentioned above, we conclude that digital clubbing can occur in the absence of hypoxia. Digital clubbing in the absence of hypoxia has been observed in two genetic disorders related to prostaglandin (PG) E2, HPGD and SLCO2A1. PGE2 synthesis is primarily regulated by the cyclooxygenase 2, which plays a critical role in the control of inflammation. A high urine PGE level in the patient was compatible with the notion that PGE2 production may be increased in LPI. The occurrence of digital clubbing in the absence of hypoxia in LPI patients with SLC7A7 may be attributed to the mechanism of increased PGE2 production.
(Copyright © 2024 The Authors. Published by Elsevier Masson SAS.. All rights reserved.)
Databáze: MEDLINE
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