Bloch-Sulzberger syndrome


Bloch-Sulzberger syndrome, sometimes referred to as incontinentia pigmenti (IP), is a rare X-linked dominantly inherited condition that manifests at birth or in infancy. Eye problems, especially affecting the retina, are also included in it. Vascular occlusion is the cause of the retinal abnormalities, which also include exudative and tractional retinal detachments, haemorrhages, and neovascularization.



 


  • Genetic diseases
  • X chromosome
  • Pigmentation disorders
  • Visual processing

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