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Table 2 Clinical characteristics of CMT2C patients from reported cases

From: A TRPV4 mutation caused Charcot-Marie-Tooth disease type 2C with scapuloperoneal muscular atrophy overlap syndrome and scapuloperoneal spinal muscular atrophy in one family: a case report and literature review

Case number

1

2

3

4

5

6

7

8

9

10

Study

Deng et al. 2020 [10]

Sullivan et al.2015 [12]

Evangelista et al.2015 [13]

Echaniz-Laguna et al.2014 [4]

Landoure et al.2012 [14]

Klein et al. 2011 [11]

Auer-Grumbach et al.2010 [7]

Landoure et al.2010 [14]

Zimoń et al.2010 [3]

Chen et al. 2010 [16]

Number

(male)

2 (2)

4 (2)

1 (0)

1 (1)

3(1)

4(2)

9

17(6)

1 (0)

3(1)

6(2)

Mean age at onset

Childhood

33

40

Childhood

5

39

15

16

6

26/1a

7a

Family history

Incomplete penetrance

AD

De novo

De novo

AD

AD

/De novo

AD

AD

De novo

AD

AD

Mutation site

R316C

R269C

R237G R237L

D62N

R232S

R186Q

R232C R316H

R316C R315W

R269C R269H

V620I

R315W

S542Y

Sensory involvement

2/2

4/4

1/1

1/1

3/3

4/4

5/9

16/17

0/1

3/3

2/6

Proximal UL weakness

0/2

2/4

1/1

0/1

0/3

0/4

6/7

8/17

0/1

0/3

0/6

Proximal LL weakness

0/2

1/4

1/1

0/1

1/3

0/4

NA

0/1

2/3

Distal UL weakness

1/2

3/4

1/1

1/1

3/3

2/4

8/9

17/17

1/1

3/3

4/6

Distal LL weakness

2/2

4/4

1/1

1/1

3/3

2/4

9/9

0/1

Areflexia

2/2

2/4

0/1

NA

3/3

4/4

9/9

NA

NA

3/3

6/6

Scoliosis

0/2

0/4

0/1

1/1

2/3

0/4

4/7

2/5

1/1

0/3

0/6

Vocal cord paralysis

1/2

2/4

0/1

1/1

3/3

2/4

7/9

15/15

0/1

2/3

4/6

Hearing loss

1/2

0/4

0/1

0/1

1/3

0/4

NA

10/17

0/1

0/3

0/6

Pes cavus

2/2

NA

0/1

1/1

NA

1/4

NA

3/7

NA

NA

1/6

Other features

   

Tremor

 

Shortness of breath

 

Bladder incontinence

Short stature

Congenital

CN III palsy

Short stature

Dolichocephaly

  1. AD Autosomal dominant, UL Upper limb, LL Lower limb, NA Not available, CN Cranial nerve
  2. aHoarse voice/wheezing