Börjeson-Forssman-Lehmann Syndrome in a Pediatric Patient: A Four-Year Longitudinal Case Report Focused on Functional Evolution and Rehabilitation

Börjeson-Forssman-Lehmann syndrome (BFLS) is a rare X-linked neurodevelopmental disorder caused by pathogenic variants in the plant homeodomain finger protein 6 (PHF6) gene, typically associated with intellectual disability, hypotonia, dysmorphic features, endocrinological abnormalities, epilepsy, and global developmental impairment. Most published literature focuses on genetic and phenotypic characterization, with limited information regarding rehabilitation or long-term functional outcomes. We report the longitudinal follow-up of a male child with genetically confirmed BFLS, monitored from the age of 7 months (December 2021) to the age of 4.5 years (October 2025) at the time of manuscript submission, while receiving multidisciplinary rehabilitation. Interventions included physiotherapy targeting postural control and antigravity activation, occupational therapy addressing sensory regulation and purposeful reaching, speech and feeding therapy providing oral-motor stimulation and saliva management, structured caregiver training, and the prescription of assistive devices such as adaptive seating systems and a standing frame. Despite severe axial hypotonia and global developmental delay, the child achieved gradual but modest gains in head control, brief supported sitting, visually guided reaching, and social engagement. Feeding transitioned from mixed oral intake to percutaneous endoscopic gastrostomy (PEG) dependence for nutritional safety and adequacy, while minimal oral stimulation was maintained. A review of the literature confirms that rehabilitation trajectories in BFLS are rarely described and that no standardized guidelines exist. This case contributes one of the few multi-year functional follow-ups available and highlights that early, sustained, and individualized multidisciplinary rehabilitation can promote incremental improvements in motor function, interaction, even in severe presentations, with meaningful implications for quality of life.

Authors

Institutions

Publication Details

Journal
Cureus
Published
2026-01-13
DOI
https://doi.org/10.7759/cureus.101421
Primary Topic
Genomics and Rare Diseases
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Börjeson-Forssman-Lehmann Syndrome in a Pediatric Patient: A Four-Year Longitudinal Case Report Focused on Functional Evolution and Rehabilitation

Helena Reis Costa, José Pedro Pimenta, Vitor Machado Sousa, Marco Francisco Silva et al.
Cureus
Genomics and Rare Diseases
article

Börjeson-Forssman-Lehmann Syndrome in a Pediatric Patient: A Four-Year Longitudinal Case Report Focused on Functional Evolution and Rehabilitation

Helena Reis Costa, José Pedro Pimenta, Vitor Machado Sousa, Marco Francisco Silva, Raquel Sofia Santos
article en

Abstract

Börjeson-Forssman-Lehmann syndrome (BFLS) is a rare X-linked neurodevelopmental disorder caused by pathogenic variants in the plant homeodomain finger protein 6 (PHF6) gene, typically associated with intellectual disability, hypotonia, dysmorphic features, endocrinological abnormalities, epilepsy, and global developmental impairment. Most published literature focuses on genetic and phenotypic characterization, with limited information regarding rehabilitation or long-term functional outcomes. We report the longitudinal follow-up of a male child with genetically confirmed BFLS, monitored from the age of 7 months (December 2021) to the age of 4.5 years (October 2025) at the time of manuscript submission, while receiving multidisciplinary rehabilitation. Interventions included physiotherapy targeting postural control and antigravity activation, occupational therapy addressing sensory regulation and purposeful reaching, speech and feeding therapy providing oral-motor stimulation and saliva management, structured caregiver training, and the prescription of assistive devices such as adaptive seating systems and a standing frame. Despite severe axial hypotonia and global developmental delay, the child achieved gradual but modest gains in head control, brief supported sitting, visually guided reaching, and social engagement. Feeding transitioned from mixed oral intake to percutaneous endoscopic gastrostomy (PEG) dependence for nutritional safety and adequacy, while minimal oral stimulation was maintained. A review of the literature confirms that rehabilitation trajectories in BFLS are rarely described and that no standardized guidelines exist. This case contributes one of the few multi-year functional follow-ups available and highlights that early, sustained, and individualized multidisciplinary rehabilitation can promote incremental improvements in motor function, interaction, even in severe presentations, with meaningful implications for quality of life.

CureusVol. 18(1)
Administração Regional de Saúde de Lisboa e Vale do Tejo (PT)
Zero hunger
Openalex Percentile: Top 90%
Genomics and Rare Diseases
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

Börjeson-Forssman-Lehmann Syndrome in a Pediatric Patient: A Four-Year Longitudinal Case Report Focused on Functional Evolution and Rehabilitation — Helena Reis Costa, José Pedro Pimenta, et al. · Cureus (2026) | TGRS Research Map | TGRS