• A new mutation associated with Pierson syndrome
• A novel gain-of-function mutation in ORAI1 causes late-onset tubular aggregate myopathy and congenital miosis
• A Novel Homozygous Truncating Mutation in <em>LAMB2</em> Gene in a Chinese Uyghur Patient With Severe Phenotype Pierson Syndrome
• A novel mutation of laminin β2 (LAMB2) in two siblings with renal failure
• A rare case of congenital pupillary abnormality: a case report
• Acorea: A rare congenital anomaly
• An extremely mild clinical course in a case with LAMB2-associated nephritis diagnosed with next-generation sequencing
• Case of Pierson syndrome presented with hyphema,vitrous haemorrhage and subsequent neovascular glaucoma
• Case Report: Congenital Pseudoacorea in an Ocular Axenfeld-Rieger Syndrome: What is it?
• Congenital Microcoria
• Congenital microcoria in a Saudi family
• Congenital Microcoria: Clinical Features and Molecular Genetics
• Familial acorea, microphthalmia and cataract syndrome
• Five-Year Follow-Up and Successful Kidney Transplantation in a Girl with a Severe Phenotype of Pierson Syndrome
• Gastrointestinal symptoms as an extended clinical feature of Pierson syndrome: a case report and review of the literature
• Genome sequencing identifies a large deletion at 13q32.1 as the cause of microcoria and childhood-onset glaucoma
• Microcoria due to first duplication of 13q32.1 including the GPR180 gene and maternal mosaicism
• Miosis in a case of congenital fibrosis of extraocular muscles: a rare presentation of a rare disease
• Paternal isodisomy of chromosome 3 unmasked by autosomal recessive microcoria-congenital nephrosis syndrome (Pierson syndrome) in a child with no other phenotypic abnormalities
• Phacoemulsification and 1% atropine eye drops for treatment of antimetropic congenital microcoria associated with cataracts
• Pierson Syndrome Associated with Hypothyroidism and Septic Shock
• Posterior Segment Characterization in Children With Pierson Syndrome
• Rare micropupil secondary to congenital cataract surgery favoring the development of the affected eye: a case report
• Seizure-induced miosis
• Submicroscopic deletions at 13q32.1 cause congenital microcoria
• Unique Ocular Findings in an Infant with Pierson (Microcoria-Congenital Nephrosis) Syndrome