Albums and FRAME Projects tagged with "vision"

  • Smith-Magenis syndrome is a rare chromosomal disorder characterized by a specific pattern of physical, behavioral, and developmental features. It is [...]

  • Marfan syndrome is a genetic disorder that affects the body’s connective tissue. Connective tissue holds all the body’s cells, organs [...]

  • Hermansky-Pudlak Syndrome (HPS) is a genetic metabolic disorder, with a prevalence of 1 to 9 in 1,000,000 individuals worldwide. It [...]

  • Albinism is a recessive genetic condition that causes the absence or reduction of pigmentation in the hair, skin and eyes.

  • Anophthalmia is a birth defect where a baby is born without one or both eyes.

  • Cockayne Syndrome (CS) is a rare genetic disorder characterized by poor growth, microcephaly, progeria (premature aging), sensitivity to sunlight, moderate [...]

  • Albinism is a recessive genetic condition that causes the absence or reduction of pigmentation in the hair, skin and eyes.