Osteoporosis-pseudoglioma syndrome or OPGG is a rare genetic condition characterized by early-onset blindness and severe osteoporosis alongside seemingly...
10 KB (818 words) - 16:38, 20 July 2024
Osteopoikilosis Osteoporosis macrocephaly mental retardation blindness Osteoporosis oculocutaneous hypopigmentation syndrome Osteoporosis pseudoglioma syndrome Osteoporosis...
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changes in bone mass. A loss-of-function mutation causes osteoporosis pseudoglioma syndrome with a decrease in bone mass, while a gain-of-function mutation...
24 KB (3,205 words) - 21:15, 27 March 2024
for osteoporosis risk and to identify those who might benefit from measures to improve bone strength. A bone density test may detect osteoporosis or osteopenia...
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Syndromic microphthalmia is a class of rare congenital anomalies characterized by microphthalmia along with other non-ocular malformations. Syndromic...
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Pedro Pan Opponents Points per game, in sports statistics Osteoporosis-pseudoglioma syndrome, a medical condition This disambiguation page lists articles...
497 bytes (87 words) - 12:08, 13 September 2022
neurological anomalies. Osteoporosis-pseudoglioma syndrome, genetic disorder which combines the association of osteoporosis and pseudoglioma. Osteogenesis imperfecta...
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which contribute to osteoporosis. Loss of function mutations in LRP5 have been implicated in Osteoporosis-pseudoglioma syndrome, Familial exudative vitreoretinopathy...
21 KB (3,129 words) - 10:03, 2 June 2024
TCIRG1 Osteopoikilosis; 166700; LEMD3 Osteoporosis, involutional; 166710; VDR Osteoporosis-pseudoglioma syndrome; 259770; LRP5 Osteosarcoma; 259500; LOH18CR1...
234 KB (18,877 words) - 15:43, 9 May 2024