Increased Head Circumference Latest Advances

Find the Latest Research About Increased Head Circumference

Last Updated: 06/30/2026

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Found 1305 publications

Craniometaphyseal dysplasia: a rare cause of persistent macrocephaly.

Craniometaphyseal dysplasia: a rare cause of persistent macrocephaly.

Journal: BMJ case reports

Published: June 16, 2026

Homozygous R383H variant in IDUA gene causing pericentric retinitis pigmentosa in attenuated mucopolysaccharidosis type I.

Homozygous R383H variant in IDUA gene causing pericentric retinitis pigmentosa in attenuated mucopolysaccharidosis type I.

Journal: Ophthalmic genetics

Published: May 20, 2026

Epilepsy in Epidermal Nevus Syndromes: Review.

Epilepsy in Epidermal Nevus Syndromes: Review.

Journal: Journal of child neurology

Published: May 19, 2026

Vein of Galen Malformation Masquerading as Neonatal Respiratory Distress.

Vein of Galen Malformation Masquerading as Neonatal Respiratory Distress.

Journal: Cureus

Published: May 17, 2026

Carotid cavernous fistula in a young adult with Bannayan-Riley-Ruvalcaba syndrome.

Carotid cavernous fistula in a young adult with Bannayan-Riley-Ruvalcaba syndrome.

Journal: Orbit (Amsterdam, Netherlands)

Published: May 11, 2026

Mosaic Variant in Unilateral Woolly Hair in a Girl With PIK3CA-Related Overgrowth Spectrum.

Mosaic Variant in Unilateral Woolly Hair in a Girl With PIK3CA-Related Overgrowth Spectrum.

Journal: Congenital anomalies

Published: April 27, 2026

L-2-Hydroxyglutaric Aciduria Due to the Homozygous Variant c.905C>T in L2HGDH Without Cognitive Deficits or Gait Disturbance: A Case Report.

L-2-Hydroxyglutaric Aciduria Due to the Homozygous Variant c.905C>T in L2HGDH Without Cognitive Deficits or Gait Disturbance: A Case Report.

Journal: Cureus

Published: April 25, 2026

STRADA deficiency impairs cortical interneuron development in humans and mice.

STRADA deficiency impairs cortical interneuron development in humans and mice.

Journal: bioRxiv : the preprint server for biology

Published: April 10, 2026

Camurati-Engelmann disease with bilateral proptosis and optic neuropathy: a case report and literature review.

Camurati-Engelmann disease with bilateral proptosis and optic neuropathy: a case report and literature review.

Journal: Orbit (Amsterdam, Netherlands)

Published: April 08, 2026

Thanatophoric Dysplasia Type I Confirmed by Fibroblast Growth Factor Receptor 3 (FGFR3) Mutation: Clinical Course and Ethical Considerations.

Thanatophoric Dysplasia Type I Confirmed by Fibroblast Growth Factor Receptor 3 (FGFR3) Mutation: Clinical Course and Ethical Considerations.

Journal: Cureus

Published: April 02, 2026

Growth Faltering: Definitions and References for Typical Ranges.

Growth Faltering: Definitions and References for Typical Ranges.

Journal: Pediatric annals

Published: April 02, 2026

A Stepwise Approach to Macrocephaly: Clinical Clues to the Rare Diagnosis of PTEN Hamartoma Tumor Syndrome.

A Stepwise Approach to Macrocephaly: Clinical Clues to the Rare Diagnosis of PTEN Hamartoma Tumor Syndrome.

Journal: Pediatric annals

Published: April 02, 2026

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Last Updated: 06/30/2026