X-Linked Hypophosphatemia Latest Advances

Secondary Deformity After Hemiepiphysiodesis in Hypophosphatemic Rickets: The Role of Metabolic Control.

Journal: Journal of pediatric orthopedics

Published: November 11, 2025

A Rare Cause of Sacral Insufficiency Fracture in Adolescence: Autosomal Dominant Hypophosphatemic Rickets due to Fgf23 de novo P.Arg176trp Variant.

Journal: Journal of clinical research in pediatric endocrinology

Published: October 30, 2025

Correction: Experts' consensus on the management and treatment of individuals with X-linked hypophosphatemia across lifespan.

Journal: Journal of endocrinological investigation

Published: October 08, 2025

Distribution of blood pressure and its positive association with body mass index standard deviation score in pediatric patients with X-linked hypophosphatemia: a sub-group analysis from the SUNFLOWER observational study.

Journal: Endocrine journal

Published: October 05, 2025

X-Linked Hypophosphatemia in a Family Cohort: Clinical Variability, Genetic Confirmation and Modern Therapeutic Perspectives.

Journal: Journal of clinical medicine

Published: September 29, 2025

Lower Limb Deformity in Different Types of Rickets.

Journal: Journal of clinical medicine

Published: September 29, 2025

Childhood fibrous dysplasia.

Journal: Orthopaedics & traumatology, surgery & research : OTSR

Published: September 25, 2025

Proceedings of the 2025 Santa Fe Bone Symposium: Current concepts in the care of patients with osteoporosis, parathyroid disorders, and rare bone diseases.

Journal: Journal of clinical densitometry : the official journal of the International Society for Clinical Densitometry

Published: September 21, 2025

Clinical and Laboratory Characteristics of Patients with Genetic Rickets: A Single-Center Experience with Long-Term Outcomes.

Journal: Turkish archives of pediatrics

Published: September 17, 2025

Deformity Correction in an Adult With Hypophosphatemic Rickets.

Journal: Cureus

Published: September 16, 2025

Two-year structural skeletal outcomes of burosumab therapy in pediatric X-linked hypophosphatemia: A radiographic cohort study.

Journal: Journal of children's orthopaedics

Published: September 08, 2025

Treatment-Resistant Hypophosphataemia After Ferric Carboxymaltose: Expanding the Spectrum of 6h Syndrome (Hypophosphataemia, Hyperphosphaturia, Hypovitaminosis D, Hypocalcaemia, Secondary Hyperparathyroidism, High Fibroblast Growth Factor-23).

Journal: European journal of case reports in internal medicine

Published: September 05, 2025

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Secondary Deformity After Hemiepiphysiodesis in Hypophosphatemic Rickets: The Role of Metabolic Control.

Secondary Deformity After Hemiepiphysiodesis in Hypophosphatemic Rickets: The Role of Metabolic Control.

A Rare Cause of Sacral Insufficiency Fracture in Adolescence: Autosomal Dominant Hypophosphatemic Rickets due to Fgf23 de novo P.Arg176trp Variant.

A Rare Cause of Sacral Insufficiency Fracture in Adolescence: Autosomal Dominant Hypophosphatemic Rickets due to Fgf23 de novo P.Arg176trp Variant.

Correction: Experts' consensus on the management and treatment of individuals with X-linked hypophosphatemia across lifespan.

Correction: Experts' consensus on the management and treatment of individuals with X-linked hypophosphatemia across lifespan.

Distribution of blood pressure and its positive association with body mass index standard deviation score in pediatric patients with X-linked hypophosphatemia: a sub-group analysis from the SUNFLOWER observational study.

Distribution of blood pressure and its positive association with body mass index standard deviation score in pediatric patients with X-linked hypophosphatemia: a sub-group analysis from the SUNFLOWER observational study.

X-Linked Hypophosphatemia in a Family Cohort: Clinical Variability, Genetic Confirmation and Modern Therapeutic Perspectives.

X-Linked Hypophosphatemia in a Family Cohort: Clinical Variability, Genetic Confirmation and Modern Therapeutic Perspectives.

Lower Limb Deformity in Different Types of Rickets.

Lower Limb Deformity in Different Types of Rickets.

Childhood fibrous dysplasia.

Childhood fibrous dysplasia.

Proceedings of the 2025 Santa Fe Bone Symposium: Current concepts in the care of patients with osteoporosis, parathyroid disorders, and rare bone diseases.

Proceedings of the 2025 Santa Fe Bone Symposium: Current concepts in the care of patients with osteoporosis, parathyroid disorders, and rare bone diseases.

Clinical and Laboratory Characteristics of Patients with Genetic Rickets: A Single-Center Experience with Long-Term Outcomes.

Clinical and Laboratory Characteristics of Patients with Genetic Rickets: A Single-Center Experience with Long-Term Outcomes.

Deformity Correction in an Adult With Hypophosphatemic Rickets.

Deformity Correction in an Adult With Hypophosphatemic Rickets.

Two-year structural skeletal outcomes of burosumab therapy in pediatric X-linked hypophosphatemia: A radiographic cohort study.

Two-year structural skeletal outcomes of burosumab therapy in pediatric X-linked hypophosphatemia: A radiographic cohort study.

Treatment-Resistant Hypophosphataemia After Ferric Carboxymaltose: Expanding the Spectrum of 6h Syndrome (Hypophosphataemia, Hyperphosphaturia, Hypovitaminosis D, Hypocalcaemia, Secondary Hyperparathyroidism, High Fibroblast Growth Factor-23).

Treatment-Resistant Hypophosphataemia After Ferric Carboxymaltose: Expanding the Spectrum of 6h Syndrome (Hypophosphataemia, Hyperphosphaturia, Hypovitaminosis D, Hypocalcaemia, Secondary Hyperparathyroidism, High Fibroblast Growth Factor-23).