Leukoencephalopathy and conduction blocks in PLEKHG5-associated intermediate CMT disease - Sorbonne Université
Journal Articles Neuromuscular Disorders Year : 2021

Leukoencephalopathy and conduction blocks in PLEKHG5-associated intermediate CMT disease

Abstract

Biallelic variants in PLEKHG5 have been reported so far associated with different clinical phenotypes including Lower motor neuron disease (LMND) [also known as distal hereditary motor neuropathies (dHMN or HMN) or distal spinal muscular atrophy (DSMA4)] and intermediate Charcot-Marie-Tooth disease (CMT). We report four patients from two families presenting with intermediate CMT and atypical clinical and para-clinical findings. Patients presented with predominant distal weakness with none or mild sensory involvement and remain ambulant at last examination (22–36 years). Nerve conduction studies revealed, in all patients, intermediate motor nerve conduction velocities, reduced sensory amplitudes and multiple conduction blocks in upper limbs, outside of typical nerve compression sites. CK levels were strikingly elevated (1611–3867 U/L). CSF protein content was mildly elevated in two patients. Diffuse bilateral white matter lesions were detected in one patient. Genetic analysis revealed three novel frameshift variants c.1835_1860del and c.2308del (family 1) and c.104del (family 2). PLEKHG5-associated disease ranges from pure motor phenotypes with predominantly proximal involvement to intermediate CMT with predominant distal motor involvement and mild sensory symptoms. Leukoencephalopathy, elevated CK levels and the presence of conduction blocks associated with intermediate velocities in NCS are part of the phenotype and may arise suspicion of the disease, thus avoiding misdiagnosis and unnecessary therapeutics in these patients.
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Dates and versions

hal-03285057 , version 1 (13-07-2021)

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Nguyen Thi Huong, Rocio-Nur Villar-Quiles, Van Thuy Le, Sarah Leonard-Louis, Lilia Laddada, et al.. Leukoencephalopathy and conduction blocks in PLEKHG5-associated intermediate CMT disease. Neuromuscular Disorders, 2021, ⟨10.1016/j.nmd.2021.06.004⟩. ⟨hal-03285057⟩
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