Transient, recurrent, white matter lesions in x-linked Charcot-Marie-tooth disease with novel mutation of gap junction protein beta 1 gene in China: a case report
© Zhao et al.; licensee BioMed Central Ltd. 2014
Received: 25 August 2013
Accepted: 24 July 2014
Published: 3 August 2014
Transient white matter lesions have been rarely reported in X-linked Charcot-Marie-Tooth disease type 1.
We describe a 15-year-old boy who presented transient and recurrent weakness of the limbs for 5 days. His mother, his mother’s mother and his mother’s sister presented pes cavus. MRI and electrophysiology were performed in the proband. Gap junction protein beta l gene was analyzed by PCR-sequencing in the proband and his parents. The electrophysiological studies showed a mixed demyelinating and axonal sensorimotor neuropathy. MRI showed white matter lesions in the internal capsule, corpus callosum and periventricular areas, which showed almost complete resolution after two months. T278G mutation in Gap junction protein beta l gene was detected in the proband and his mother.
This case report highlights that the novel T278G mutation of Gap junction protein beta l maybe could result in X-linked Charcot-Marie-Tooth disease type 1 with predominant leucoencephalopathy. The white matter changes in MRI of X-linked Charcot-Marie-Tooth disease type 1 patient are reversible.
KeywordsCharcot-Marie-Tooth disease White Matter Gap junction protein beta l Connexins Mutation
Charcot-Marie-Tooth disease (CMT) is the most frequent hereditary neurological disorder in the world, which affects 1 in 2,500 people. Most CMT diseases are autosomal dominant, the rest are recessive and X-linked forms. CMTX is divided into a dominant CMTX1 and four recessive CMTX2–5. CMTX accounts for approximately 10%-20% of all hereditary demyelinating neuropathies .
CMTX is characterized by distal muscle weakness and atrophy with characteristic steppage gait,pes cavus, decreased deep tendon reflexes and sensory loss. Recently, transient white matter lesions in CMTX have been reported, and become a prominent clinical manifestation. CMTX is caused by mutation in the GJB1 gene on chromosome Xq13.1 that codes for the connexin 32 protein (Cx32). Cx32 is expressed in the myelinating Schwann cells of the peripheral nerves. However, the protein is also widely expressed in the oligodendrocyte of the central nervous system (CNS). Cx32 maintains the permeability of myelinating cells . CX32 plays an important an role in the biology of myelin-forming cells Cx32 maintains the permeability of neurons. We analyse a CMTX male patient by the clinical manifestations, imagings and genetic analyses, who developed transient CNS dysfunction accompanied by a Cx32 mutation and diffuse white matter abnormalities.
A 15-year-old male of Han nationality presented with a sudden weakness of limbs. Five days before being admitted to our hospital, about five pm after school, the patient felt weakness of the lower limbs and walked unsteadily. However, he did not show weakness of both upper limbs, chest congestion, palpitations, dizziness, headache, numbness of the limbs, convulsion and incontinence. About five thirty pm, weakness of his both lower limbs disappeared. But he showed weakness of both upper limbs twice. Three days before admission, he did not write well with his right hand when he was at school. Two days before admission, he could not lift his left arm and had slurred speech, dysphagia, which lasted 2–3 hours before being recovered. On the day of admission, he presented right hemiplegia and numbness. History of past illness showed that he had a high fever two weeks before onset, the highest temperature was 39.9°C, and he was poor in spirit, but did not show cough, expectoration, sore throat or other symptoms. He was treated by Ceftriaxone sodium and dexamethasone, and he got well soon. Two months before onset, he had a history of lower extremity weakness lasting about 30 minutes. He was the product of a normal full-term pregnancy and delivery. He had no learning difficulties. His mother, his mother’s mother and his mother’s sister presented pes cavus.
His medical examination presented the atrophy of his interosseous muscles and his distal lower extremities, flat thenar muscles, poor flexibility of his hands, diminished deep tendon reflexes in all extremities, negative bilateral Babinski signs, positive bilateral Pussep signs and equinovarus. The internal medicine examination showed no abnormalities.
Nerve conduction studies
Distal latency (ms)
Amplitude (sensory in μV, motor in mV)
Left posterior tibial
Right posterior tibial
Left posterior tibial
Right posterior tibial
The patient had normal strength in all muscle groups, but the deep tendon reflexes were diminished bilaterally when he was in our department. After hospital discharge, there was no longer onset of his neurological symptoms.
The patient in this case had hyperpyrexia two weeks before onset of the disease. The clinical manifestations showed repeated transient weakness of the limbs, slurred speech and dysphagia. Neurologic examination revealed muscular atrophy of distal limbs, diminished deep tendon reflexes in all extremities and giving the characteristic inverted champagne bottle appearance. Brain MRI scans presented white matter abnormalities in the internal capsule, corpus callosum and periventricular areas. Two months later,his third brain MRI showed that the signal abnormalities had almost disappeared. Electrophysiology certified peripheral neuropathy. The genetic analysis showed a pathogenic mutation in GJB1. This patient was diagnosed as CMTX1 accompanied by reversibility transient white matter abnormalities.
CMT is classified as autosomal dominant, autosomal recessive or X-linked CMT (CMTX). CMTX is divided into a dominant CMTX1 and four recessive CMTX 2–5 . At present we think that CMTX1 is caused by mutation in the GJB1 gene on chromosome Xq13.1 at codes for the connexin 32 protein (Cx32). Cx32 is expressed in myelinating Schwann cells and localized to paranodal regions and Schmidt Lanternmann incisures. Six connexins oligomerize to form hemichannels or connexons. When properly opposed to each other on cell membranes, two connexons form gap junction channels that permit the diffusion of ions and small molecules . The diffusion of ions and small molecules may be restricted by Cx32 mutation, which causes the defect of nervous functions.
Case reports show that transient cerebral white matter lesions of CMXT1 can be acute or subacute ataxia, dysarthria, hypoesthesia, aphasia, hemiplegia or quadriplegia etc., which can be alleviated in several hours or several days, or maybe attack repeatedly. Usually the CMXT1 symptoms are severe in male patients, but asymptomatic or mild in female carriers . Although there are reports of some female heterozygotes who have serious manifestations .
Predisposing factors to transient cerebral white matter lesions of CMXT1 may be return to plain from high altitude area, fever, infection, can even be no clear reason ,–. The CMTX1 typical MRI shows abnormalities in non-enhanced, confluent, symmetrical corpus callosum and periventricular white matter . These episodes may be related to temporary myelin vacuolation as suggested by restricted diffusion in the affected areas on MRI. Using transgenic mice shows that the mutation of Cx32 loses its function in Schwann cells and oligodendrocytes, resulting in myelination defects of the peripheral and central nervous system . Dysfunctional gap junctions as a result of the mutation enables these cells have no ability to adjust fluid exchange, these could explain the restricted diffusion on MRI . Follow-ups and literature reports about cerebral white matter lesions present that brain MRI can be fully recovered or improved in hours, days or months.
This paper reports the electrophysiological examination of the patient, which presents that the peripheral nerve axon and myelin sheath are involved. It is also reported previously that axon and myelin sheath can be involved at the same time , or the axon is involved mainly .
The male patient with novel T278G mutation of GJB1 had hemizygous, and his mother had heterozygous mutation. His mother, his mother’s mother and his mother’s sister presented pes cavus. His father had normal sequence. The CMTX1 has been known to be an X-linked dominant inheritance pattern. In CMTX, male patients tend to be severely affected, and females are generally asymptomatic . The GJBl mutation in the male patient results in the change of met93arg. We speculate that the mutation may lead to loss of functional gap junction protein in Schwann cells and oligodendrocytes, which causes the dysfunction in central nervous system.
We reported a T278G mutation causing a methionine to arginine substitution on code 93 (M93A). Bell et al.  presented a A277G mutation on code 93 (M93V). Both mutations affected the same amino acid (methionine). The clinical manifestations of M93V included tremor, spasticity, brisk reflexes and extensor plantar responses. On MRI there was atrophy of the cerebral cortex and cerebellum. While the phenotype of M93A presented transient and recurrent weakness of the limbs and diminished deep tendon reflexes in all extremities. MRI showed reversibility white matter lesions in the internal capsule, corpus callosum and periventricular areas.
In conclusion, T278G is a new mutation in the GJBl gene, which may be associated with CMTX1. The disease shows paroxysmal leukoencephalopathy. Axonal and myelin lesions result in weakness of limbs, slurred speech, swallowing difficulties. Reversible cerebral white matter damages of corpus callosum and periventricular areas are the characteristics of the disease on MRI. For patients who have peripheral nerve damages and reversible cerebral white matter degeneration, CMTX1 should be considered.
Written informed consent was obtained from the patient’s parent for publication of this Case report and any accompanying images. A copy of the written consent is available for review by the Editor of this journal.
X-linked Charcot-Marie-Tooth disease type 1
Magnetic resonance imaging
Gap junction protein beta l
Polymerase Chain Reaction
Central nervous system
Connxin 32 protein
Brain-stem auditory evoked potential
- Ionasescu V, Ionasescu R, Searby C: Correlation between connexin 32 gene mutations and clinical phenotype in X-linked dominant Charcot-Marie-Tooth neuropathy. Am J Med Genet. 1996, 63: 486-491. 10.1002/(SICI)1096-8628(19960614)63:3<486::AID-AJMG14>3.0.CO;2-I.View ArticlePubMedGoogle Scholar
- Scherer SS, Deschênes SM, Xu YT, Grinspan JB, Fischbeck KH, Paul DL: Connexin 32 a myelin-related protein in the PNS and CNS. J Neurosci. 1995, 15: 8281-8294.PubMedGoogle Scholar
- Kim Y, Choi KG, Park KD, Lee KS, Chung KW, Choi BO: X-linked dominant Charcot-Marie-Tooth disease with connexin 32 (Cx32) mutations in Koreans. Clin Genet. 2012, 81 (2): 142-149. 10.1111/j.1399-0004.2011.01642.x.View ArticlePubMedGoogle Scholar
- Paulson HL, Garbern JY, Hoban TF, Krajewski KM, Lewis RA, Fischbeck KH, Grossman RI, Lenkinski R, Kamholz JA, Shy ME: Transient central nervous system white matter abnormality in X-linked Charcot-Marie-Tooth disease. Ann Neurol. 2002, 52: 429-434. 10.1002/ana.10305.View ArticlePubMedGoogle Scholar
- Anand G, Maheshwari N, Roberts D, Padeniya A, Hamilton-Ayers M, van der Knaap M, Fratter C, Jayawant S: X-linked hereditary motor sensory neuropathy (type 1) presenting with a stroke-like episode. Dev Med Child Neurol. 2010, 52 (7): 677-679. 10.1111/j.1469-8749.2010.03674.x.View ArticlePubMedGoogle Scholar
- Basri R, Yabe I, Soma H, Matsushima M, Tsuji S, Sasaki H: X-linked Charcot-Marie-Tooth Disease (CMTX) in a severely affected female patient with scattered lesions in cerebral white matter. Intern Med. 2007, 46: 1023-1027. 10.2169/internalmedicine.46.0047.View ArticlePubMedGoogle Scholar
- Schelhaas HJ, Van Engelen BG, Gabreëls-Festen AA, Hageman G, Vliegen JH, Van Der Knaap MS, Zwarts MJ: Transient cerebral white matter lesions in a patient with connexin 32 missense mutation. Neurology. 2002, 59: 2007-2008. 10.1212/01.WNL.0000038390.29853.46.View ArticlePubMedGoogle Scholar
- Hanemann CO, Bergmann C, Senderek J, Zerres K, Sperfeld AD: Transient, recurrent white matter lesions in X-linked Charcot-Marie-Tooth disease with novel connexion 32 mutation. Arch Neurol. 2003, 60: 605-609. 10.1001/archneur.60.4.605.View ArticlePubMedGoogle Scholar
- Taylor RA, Simon EM, Marks HG, Scherer SS: The CNS phenotype of X-linked Charcot-Marie-Tooth disease: more than a peripheral problem. Neurology. 2003, 61: 1475-1478. 10.1212/01.WNL.0000095960.48964.25.View ArticlePubMedGoogle Scholar
- Isoardo G, Di Vito N, Nobile M, Benetton G, Fassio F: X-linked Charcot-Marie - Tooth disease and progressive-relapsing central demyelinating disease. Neurology. 2005, 65: 1672-1673. 10.1212/01.wnl.0000186032.06791.94.View ArticlePubMedGoogle Scholar
- Sargiannidou I, Vavlitou N, Aristodemou S, Hadjisavvas A, Kyriacou K, Scherer SS, Kleopa KA: Connexin 32 mutations cause loss of function in Schwann cells and oligodendrocytes leading to PNS and CNS myelination defects. J Neurosci. 2009, 29: 4736-4749. 10.1523/JNEUROSCI.0325-09.2009.View ArticlePubMedPubMed CentralGoogle Scholar
- Senderek J, Hermanns B, Bergmann C, Boroojerdi B, Bajbouj M, Hungs M, Ramaekers VT, Quasthoff S, Karch D, Schröder JM: X-linked dominant Charoot-Marie-Tooth neuropathy: clinical, electrophysiological, and morphological phenotype in four families with different connexin32 mutations. J Neurol Sci. 1999, 167: 90-101. 10.1016/S0022-510X(99)00146-X.View ArticlePubMedGoogle Scholar
- Marques W, Sweeney JG, Wood NW, Wroe SJ, Marques W: Central nervous system involvement in a novel connexin 32 mutation affecting identical twins. J Neurol Neurosurg Psychiatry. 1999, 66 (6): 803-804. 10.1136/jnnp.66.6.803.View ArticlePubMedPubMed CentralGoogle Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited.