CMT2T

MME | 2016

Illustration of a DNA double helix overlaid on nerve cells, with text reading ‘Experts in CMT: CMT Genes and Subtypes Database

CMT2T is caused by mutations in the MME gene. This gene provides instructions for producing membrane metalloendopeptidase, an enzyme involved in the breakdown of neuropeptides and regulation of signaling at the cell surface. Mutations in the MME gene disrupt normal peptide processing in peripheral nerve cells, leading to impaired axonal function and nerve signal transmission.

CMT2T can be either autosomal dominant or autosomal recessive, meaning that sometimes it’s just one of the gene’s two copies with a CMT-causing mutation, and sometimes it’s both copies.

Clinical Features

CMT2T is a late-onset subtype with symptoms typically beginning in the thirties and later. Symptoms typically begin in the lower extremities and progress over time to involve the upper limbs. Nerve conduction studies usually show somewhat slowed conduction velocities and reduced amplitudes, consistent with an axonal form of CMT.

CMT2T symptoms may include:

  • Weakness in the feet and lower legs
  • Muscle atrophy
  • Foot drop
  • A steppage-style walking pattern
  • Reduced sensation
  • Reduced or absent reflexes
  • Foot deformities, including high arches and hammertoes (clawed toes)
  • Progressive involvement of the hands and forearms
  • Difficulty with fine motor skills and manual dexterity
  • Balance difficulties
  • Additional symptoms not listed here

Disease Course

CMT2T shows wide variability in severity and progression. Some individuals are mildly affected, while others develop a more severe disease. Patients with a single, pathogenic heterozygous MME gene mutation typically have a later onset. Disease progression is generally slow, and life expectancy is not reduced.

Clinical Basics

Subtype
CMT2T

Classification
CMT2

Neuropathy Type
Axonal

Inheritance Pattern
Autosomal Dominant, Autosomal Recessive

Genetic Context

HGNC-Approved Gene Symbol
MME

Gene Full Name
Membrane Metalloendopeptidase

HGNC Gene Alias(es)
CALLA, CD10, NEP

Chromosome
3q25.2

Zygosity of Responsible Variant
Heterozygous or Homozygous or Compound Heterozygous

Mitochondrial Involvement
No

ClinVar Pathogenic Variants

View CMT2T ClinVar Variants

More Info

Research Opportunity

CMT Natural History Study

Original Discovery Publications

Note:

This is the original publication for CMT2T, which is autosomal recessive MME variants (AR-CMT2T).

Publication Title

Mutations in MME cause an autosomal-recessive Charcot-Marie-Tooth disease type 2.

Authors

Higuchi, Y., Hashiguchi, A., Yuan, J., Yoshimura, A., Mitsui, J., Ishiura, H., Tanaka, M., Ishihara, S., Tanabe, H., Nozuma, S., Okamoto, Y., Matsuura, E., Ohkubo, R., Inamizu, S., Shiraishi, W., Yamasaki, R., Ohyagi, Y., Kira, J., Oya, Y., Yabe,Nishikawa, N., Tobisawa, S., Matsuda, N., Masuda, M., Kugimotot, C., Fukushima, K., Yano, S., Yoshimura, J., Doi, K., Nakagawa, M., Morishita, S., Tsuji, S., H.,  Takashima, H.

Publication Date
April 8, 2016

Note:

This publication identified autosomal dominant MME variants causing CMT2K (AD-CMT2T).

Publication Title

Rare Variants in MME, Encoding Metalloprotease Neprilysin, Are Linked to Late-Onset Autosomal-Dominant Axonal Polyneuropathies

Authors

Auer-Grumbach, M., Toegel, S., Schabhüttl, M., Weinmann, D., Chiari, C., Bennett, D., Beetz, C., Klein, D., Andersen, P. M., Böhme, I., Fink-Puches, R., Gonzalez, M., Harms, M. B., Motley, W., Reilly, M. M., Renner, W., Rudnik-Schöneborn, S., Schlotter-Weigel, B., Themistocleous, A. C., Weishaupt, J. H., Ludolph, A.C., Wieland, T., Tao, F., Abrue, L., Windhager, R., Zitzelsberger, M., Strom., T.M., Walther, T., Scherer, S.S., Züchner, S., Martini, R., Senderek, J.

Publication Date
September 1, 2016

Updated: February 7, 2026 | By: K. Raymond

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