Tag: NSDHL gene


BORJESON-FORSSMAN-LEHMANN SYNDROME

Borjeson-Forssman-Lehmann Syndrome Introduction: What is Borjeson-Forssman-Lehmann Syndrome (BFLS)? Börjeson-Forssman-Lehmann syndrome (BFLS) is a rare, inherited X-linked genetic disorder primarily characterized by a complex constellation of symptoms including intellectual disability, recurrent seizures, and distinctive dysmorphic facial features. This syndrome represents a profound challenge to affected individuals and their families, impacting various aspects of physical and cognitive […]

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