Results 131 to 140 of about 2,813 (161)
Some of the next articles are maybe not open access.
Clinical Pediatrics, 1974
A case of ectopia lentis et pupillae in a nine-month-old male is presented. This entity is an autosomal recessive disorder characterized by displacement of the pupils and lens. Marfan's syndrome, homocystinuria, Marchesani syn drome, hereditary microspherophakia, and Ehlers-Danlos syndrome are included in the differential diagnoses of displaced lens ...
openaire +2 more sources
A case of ectopia lentis et pupillae in a nine-month-old male is presented. This entity is an autosomal recessive disorder characterized by displacement of the pupils and lens. Marfan's syndrome, homocystinuria, Marchesani syn drome, hereditary microspherophakia, and Ehlers-Danlos syndrome are included in the differential diagnoses of displaced lens ...
openaire +2 more sources
American Journal of Ophthalmology, 1979
Two brothers whose parents were second cousins had ectopia lentis et pupillae. This autosomal recessive disorder is distinguished from other disorders with ectopia lentis by the limitation of abnormalities to the bilateral displacement of lens and pupil.
openaire +2 more sources
Two brothers whose parents were second cousins had ectopia lentis et pupillae. This autosomal recessive disorder is distinguished from other disorders with ectopia lentis by the limitation of abnormalities to the bilateral displacement of lens and pupil.
openaire +2 more sources
Ectopia lentis in homocystinuria
Journal Français d'Ophtalmologie, 2019I, Sabrane +6 more
openaire +2 more sources
Archives of Ophthalmology, 1976
Two brothers had ectopia lentis et pupillae, an autosomal recessive disorder. Ascertainment of the brothers occurred through an unaffected sister, who sought genetic advice concerning possible risk for the disorder in her future children. Although the clinical features and the genetic aspects of ectopia lentis et pupillae are well documented in the ...
openaire +2 more sources
Two brothers had ectopia lentis et pupillae, an autosomal recessive disorder. Ascertainment of the brothers occurred through an unaffected sister, who sought genetic advice concerning possible risk for the disorder in her future children. Although the clinical features and the genetic aspects of ectopia lentis et pupillae are well documented in the ...
openaire +2 more sources
ADAMTSL4‐related ectopia lentis: A case of pseudodominance with an asymptomatic parent
American Journal of Medical Genetics, Part A, 2022Ken K Nischal, Hannah Scanga
exaly
Classifying Ectopia Lentis in Marfan Syndrome into Five Grades of Increasing Severity
Journal of Clinical Medicine, 2020Audrey Putoux +2 more
exaly
Analysis of Corneal Astigmatism before Surgery in Chinese Congenital Ectopia Lentis Patients
Current Eye Research, 2018Jianqiang Lin +2 more
exaly
Isolated congenital ectopia lentis with autosomal dominant inheritance
Clinical Genetics, 1979exaly