Synapse
⌘+K
Synapse
PulseExploreClubsResearchersJournals
Instagram
HomeClubsExplore
January 1, 2012Orphanet Journal of Rare DiseasesOpen Access

The Brown-Vialetto-Van Laere and Fazio Londe syndrome revisited: natural history, genetics, treatment and future perspectives

View Full Paper
Ask AI
Bookmark
Share

Authors

ABAnnet M. BoschEmma KinderziekenhuisKSKevin StroekAmsterdam University Medical CentersNAN. G. G. M. AbelingAmsterdam University Medical Centers

Discussion

Loading...

Member takes

Overview

Key Points

Key points are not available for this paper at this time.

Cite This Study

Bosch et al. (2012) studied this question.

synapsesocial.com/papers/6aab61ffbf7e65667fc59607https://doi.org/10.1186/1750-1172-7-83
View Full Paper
Ask AI
Bookmark
Share

Also Consider

Synapse has enriched 3 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Brown‐Vialetto‐Van Laere and Fazio Londe syndrome is associated with a riboflavin transporter defect mimicking mild MADD: a new inborn error of metabolism with potential treatment2010 · 240 citations
  2. 2Brown-Vialetto-Van Laere syndrome: Case report and literature review2000 · 27 citations
  3. 3Early use of high‐dose riboflavin in a case of Brown–Vialetto–Van Laere syndrome2011 · 71 citations