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neuropatie dedičné senzorické a motorické
Record number d015417 Date 06.06.2025 Type M Topical term neuropatie dedičné senzorické a motorické Other term Slovak (Pseudonym) Déjerineov-Sottasov syndróm
Slovak (Pseudonym) Déjerineova-Sottasova choroba
Slovak (Pseudonym) Déjerineova-Sottasova neuropatia
Slovak (Pseudonym) Déjerineova-Sottasova hypertrofická neuropatia
Slovak (Pseudonym) neuropatie dedičné motorické a senzorické
Slovak (Pseudonym) neuropatia dedičná motorická a senzorická
Slovak (Pseudonym) neuropatia dedičná motorická a senzorická 3
Slovak (Pseudonym) neuropatie hereditárne motorické a senzorické
Slovak (Pseudonym) neuropatia dedičná motorická a senzorická, typ VII
Slovak (Pseudonym) neuropatia dedičná motorická a senzorická, typ III
Slovak (Pseudonym) neuropatia proximálna dedičná motorická, typ I
Slovak (Pseudonym) HMSN
Slovak (Pseudonym) HMSN, typ III
Slovak (Pseudonym) HMSN, typ VII
Slovak (Pseudonym) HMSN3
Slovak (Pseudonym) CMT4f
Slovak (Pseudonym) Charcot-Marie-Toothova choroba, demyelinizačný typ 4f
Slovak (Pseudonym) Charcot-Marie-Toothova choroba, typ 3
UDC C10.500.300C10.574.500.495C10.668.829.800.300C16.131.666.300C16.320.400.375 Note A group of slowly progressive inherited disorders affecting motor and sensory peripheral nerves. Subtypes include HMSNs I-VII. HMSN I and II both refer to CHARCOT-MARIE-TOOTH DISEASE. HMSN III refers to hypertrophic neuropathy of infancy. HMSN IV refers to REFSUM DISEASE. HMSN V refers to a condition marked by a hereditary motor and sensory neuropathy associated with spastic paraplegia (see SPASTIC PARAPLEGIA, HEREDITARY). HMSN VI refers to HMSN associated with an inherited optic atrophy (OPTIC ATROPHIES, HEREDITARY), and HMSN VII refers to HMSN associated with retinitis pigmentosa. (From Adams et al., Principles of Neurology, 6th ed, p1343) 
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Number of the records: 1