SPHINGOSINE PHOSPHATE LYASE INSUFFICIENCY SYNDROME (SPLIS)

Clinical trials for SPHINGOSINE PHOSPHATE LYASE INSUFFICIENCY SYNDROME (SPLIS) explained in plain language.

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Rare disease mystery: can tracking SPLIS patients unlock its secrets?

Knowledge-focused Recruiting now

This study follows people with SPLIS, a rare inherited metabolic condition, to map its natural history—how the disease unfolds over time. Researchers will track growth, organ function, quality of life, and survival in about 28 participants. The goal is to understand the full rang…

Matched conditions: SPHINGOSINE PHOSPHATE LYASE INSUFFICIENCY SYNDROME (SPLIS)

Sponsor: University of California, San Francisco • Aim: Knowledge-focused

Last updated Aug 06, 2026 00:00 UTC

SPHINGOSINE PHOSPHATE LYASE INSUFFICIENCY SYNDROME (SPLIS)

Get alerted when new SPHINGOSINE PHOSPHATE LYASE INSUFFICIENCY SYNDROME (SPLIS) trials appear

Rare disease mystery: can tracking SPLIS patients unlock its secrets?