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2,069 Possible Causes for Charcot Marie Tooth Disease

  • Neuropathy

    Charcot-Marie-Tooth disease comprises a vast array of defects in myelin integrity that causes progressive peripheral sensorimotor neuropathy.[] Compound heterozygous PMP22 deletion mutations causing severe Charcot-Marie-Tooth disease type 1.[] Certain neuropathies are inherited, such as those associated with Charcot-Marie-Tooth disease, a type of hereditary neurological disorder.[]

  • Peripheral Neuropathy

    […] augmentation of prosthetic limbs has been adapted for individuals with PN and evaluated in a pilot group of 4 participants with idiopathic bilateral PN, as well as one with Charcot-Marie-Tooth[] […] neuropathy; the signs and symptoms; the evaluations and tests; and the treatment options currently known: Idiopathic Pre-diabetic/Diabetic Pre-diabetic Diabetic Hereditary Charcot-Marie-Tooth[] Inherited neuropathies such as Charcot Marie Tooth disease are also common. However, in many cases, no underlying disorder can be diagnosed.[]

  • Talipes Cavus

    Typically, with Charcot-Marie-Tooth disease, the anterior compartment muscles (tibialis anterior) are weak.[] Charcot-Marie-Tooth disease can cause painful foot deformities such as pes cavus.[] By adulthood, Charcot-Marie-Tooth disease can cause painful foot deformities such as pes cavus.[]

  • Polyneuropathy

    Charcot-Marie-Tooth Disease is the most common cause of hereditary Polyneuropathy.[] Charcot-Marie-Tooth disease is the most common form of hereditary neuropathy.[] […] scoliosis and hammer toes The causes of polyneuropathy can be divided into hereditary and acquired and are therefore as follows: Inherited -are hereditary motor neuropathies, CharcotMarieTooth[]

  • Foot Deformity

    Abstract Operative correction of cavovarus foot deformity in Charcot-Marie-Tooth disease (CMT) is challenging.[] We describe our radiographic and pedobarographic outcomes of surgical treatment of cavovarus foot deformity in children with Charcot-Marie-Tooth disease.[] Summary Charcot-Marie Tooth (CMT) disease is a condition that commonly produces a high arched foot (Figure 1).[]

  • Hereditary Motor and Sensory Neuropathy

    Therefore, diagnosing Charcot-Marie-Tooth disease can be challenging.[] Charcot-Marie-Tooth disease (hereditary motor sensory neuropathy) Progression of Charcot-Marie-Tooth disease (hereditary motor sensory neuropathy) Symptoms of Charcot-Marie-Tooth[] Background: Charcot-Marie-Tooth disease (CMT) comprises a large variety of different forms of motor and sensory neuropathies.[]

  • Dilated Cardiomyopathy Type 2B

    We discuss the current understanding of the relationship between Charcot-Marie-Tooth disease and cardiac irregularities.[] disease type 1D - CMT1D Charcot-Marie-Tooth disease type 4H - CMT4H Charcot-Marie-Tooth disease - CMT Charcot-Marie-Tooth disease axonal type 2M - CMT2M Charcot-Marie-Tooth[] Disorder LIPA Cholesteryl ester storage disease/ Wolman disease 278000 LSD Lysosomal Storage Disorder LITAF Charcot-Marie-Tooth disease, type 1C 601098 CMT Charcot-Marie-Tooth[]

  • Distal Hereditary Motor Neuropathy Type 1

    Historical note and terminology The Charcot-Marie-Tooth disease entity was recognized independently in Great Britain and France ( Charcot and Marie 1886 ; Tooth 1886 ).[] CLASSIFICATION OF CHARCOTMARIETOOTH DISEASE AND RELATED NEUROPATHIES View Table Favorite Table Download (.pdf) TABLE 11-1.[] Review Topic QID: 415 3 Charcot-Marie-Tooth Disease ML 1 Select Answer to see Preferred Response PREFERRED RESPONSE 3 (OBQ06.83) A 42-year-old woman with Charcot-Marie-Tooth[]

  • Young Adult-Onset Distal Hereditary Motor Neuropathy

    disease type 2A (CMT2A), Charcot-Marie-Tooth disease type 2B (CMT2B), Charcot-Marie-Tooth disease type 2D (CMT2D), Charcot-Marie-Tooth disease type 2E (CMT2E), CMT2, amyotrophic[] A novel TFG mutation causes Charcot-Marie-Tooth disease type 2 and impairs TFG function.[] […] due to LAMP-2 deficiency Autosomal dominant Charcot-Marie-Tooth disease type 2F 17p13.3 microduplication syndrome Distal 17p13.3 microdeletion syndrome Miller-Dieker syndrome[]

  • X-linked Distal Spinal Muscular Atrophy Type 3

    disease type 2D Autosomal dominant Charcot-Marie-Tooth disease type 2N Autosomal recessive intermediate Charcot-Marie-Tooth disease type B Cerebellar ataxia - hypogonadism[] […] motor AD 2 HSPB8 Charcot-Marie-Tooth disease, Distal hereditary motor neuronopathy AD 6 9 IGHMBP2 Spinal muscular atrophy, distal, Charcot-Marie-Tooth disease AR 52 128 LAS1L[] Disease, Axonal, Type 2N Charcot-Marie-Tooth Disease, Axonal, Autosomal Dominant, Type 2N Charcot-Marie-Tooth Neuropathy, Axonal, Type 2N CMT2N 613287 Genetic Test Registry[]

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