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Results: 7

1.

Charcot-Marie-Tooth disease, type IE

Charcot-Marie-Tooth neuropathy type 1 (CMT1) is a demyelinating peripheral neuropathy characterized by distal muscle weakness and atrophy, sensory loss, and slow nerve conduction velocity. It is usually slowly progressive and often associated with pes cavus foot deformity and bilateral foot drop. Affected individuals usually become symptomatic between age five and 25 years. Fewer than 5% of individuals become wheelchair dependent. Life span is not shortened. [from GeneReviews]

MedGen UID:
348419
Concept ID:
C1861669
Disease or Syndrome
2.

Charcot-Marie-Tooth disease, type ID

Charcot-Marie-Tooth neuropathy type 1 (CMT1) is a demyelinating peripheral neuropathy characterized by distal muscle weakness and atrophy, sensory loss, and slow nerve conduction velocity. It is usually slowly progressive and often associated with pes cavus foot deformity and bilateral foot drop. Affected individuals usually become symptomatic between age five and 25 years. Fewer than 5% of individuals become wheelchair dependent. Life span is not shortened. [from GeneReviews]

MedGen UID:
334709
Concept ID:
C1843247
Disease or Syndrome
3.

Charcot-Marie-Tooth disease, type IF

MedGen UID:
334337
Concept ID:
C1843164
Disease or Syndrome
4.

Charcot-Marie-Tooth disease, type IC

Charcot-Marie-Tooth neuropathy type 1 (CMT1) is a demyelinating peripheral neuropathy characterized by distal muscle weakness and atrophy, sensory loss, and slow nerve conduction velocity. It is usually slowly progressive and often associated with pes cavus foot deformity and bilateral foot drop. Affected individuals usually become symptomatic between age five and 25 years. Fewer than 5% of individuals become wheelchair dependent. Life span is not shortened. [from GeneReviews]

MedGen UID:
331363
Concept ID:
C1832775
Disease or Syndrome
5.

Charcot-Marie-Tooth disease, type I

Charcot-Marie-Tooth (CMT) hereditary neuropathy refers to a group of disorders characterized by a chronic motor and sensory polyneuropathy. The affected individual typically has distal muscle weakness and atrophy often associated with mild to moderate sensory loss, depressed tendon reflexes, and high-arched feet. [from GeneReviews]

MedGen UID:
155486
Concept ID:
C0751036
Disease or Syndrome
6.

Charcot-Marie-Tooth disease, type IB

Charcot-Marie-Tooth neuropathy type 1 (CMT1) is a demyelinating peripheral neuropathy characterized by distal muscle weakness and atrophy, sensory loss, and slow nerve conduction velocity. It is usually slowly progressive and often associated with pes cavus foot deformity and bilateral foot drop. Affected individuals usually become symptomatic between age five and 25 years. Fewer than 5% of individuals become wheelchair dependent. Life span is not shortened. [from GeneReviews]

MedGen UID:
124377
Concept ID:
C0270912
Disease or Syndrome
7.

Charcot-Marie-Tooth disease, type IA

Charcot-Marie-Tooth neuropathy type 1 (CMT1) is a demyelinating peripheral neuropathy characterized by distal muscle weakness and atrophy, sensory loss, and slow nerve conduction velocity. It is usually slowly progressive and often associated with pes cavus foot deformity and bilateral foot drop. Affected individuals usually become symptomatic between age five and 25 years. Fewer than 5% of individuals become wheelchair dependent. Life span is not shortened. [from GeneReviews]

MedGen UID:
75727
Concept ID:
C0270911
Disease or Syndrome

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