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Titlebook: Rare Diseases and Syndromes of the Spinal Cord; Ibrahim M. Eltorai Book 2016 Springer International Publishing Switzerland 2016 rare disea

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樓主: cherub
11#
發(fā)表于 2025-3-23 11:07:53 | 只看該作者
Anterior Arch Aplasia with OS OdontoideumThis is a condition where there is aplasia of anterior arch of atlas with os odontoideum (bipartite atlas). It is usually associated with posterior arch midline defect.
12#
發(fā)表于 2025-3-23 17:43:32 | 只看該作者
13#
發(fā)表于 2025-3-23 19:21:44 | 只看該作者
14#
發(fā)表于 2025-3-24 02:14:07 | 只看該作者
15#
發(fā)表于 2025-3-24 05:14:51 | 只看該作者
Intradural Extramedullary Capillary HemangiomaCapillary hemangiomas are reddish-purple lesions and microscopically by the lobules of capillary-sized channels that are tightly aggregated into nodules nourished by feeding vessels.
16#
發(fā)表于 2025-3-24 08:55:11 | 只看該作者
Spinal Intradural Cerebellar EctopiaThis is a condition in which cerebellar tissue is found in the spinal canal intradurally. It is independent from the Chiari I malformation, where the cerebellar tonsils are found in the upper cervical canal and from Chiari II, where the vermis is herniated in the spinal canal.
17#
發(fā)表于 2025-3-24 12:52:20 | 只看該作者
18#
發(fā)表于 2025-3-24 17:25:30 | 只看該作者
19#
發(fā)表于 2025-3-24 19:50:35 | 只看該作者
Compression Myelopathy Due to an Intramedullary Cyst Containing Ectopic Choroidal Plexus TissueThis is a unique condition where there is ectopic choroid tissue in the spinal cord causing pressure myelopathy.
20#
發(fā)表于 2025-3-24 23:20:14 | 只看該作者
Chiari 1 Malformation and Holocord Syringomyelia in Hunter SyndromeHunter syndrome, mucopolysaccharidosis type II, MPS-II, or iduronate-2-sulphatase deficiency is cause by deficiency of enzyme L-iduronate-2-sulphate. Hunter syndrome has two clinical subtypes. It shows X-linked recessive inheritance and is the only one of mucopolysacchariodosis in which the mother alone can pass the defective gene to the son.
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