The 20 Best Megalencephalic Leukoencephalopathy with Subcortical Cysts Doctors in Malta

Find the Top Megalencephalic Leukoencephalopathy with Subcortical Cysts Experts and Specialists

Last Updated: 04/28/2026

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MediFind found 1 doctor with experience in Megalencephalic Leukoencephalopathy with Subcortical Cysts near Malta. Of these, 1 are Experienced.

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1 provider found
    Experienced in Megalencephalic Leukoencephalopathy with Subcortical Cysts

    Mauro Pessia
    Experienced in Megalencephalic Leukoencephalopathy with Subcortical Cysts

    Mauro Pessia
    Imsida, MT 

    Mauro Pessia practices practicing medicine in Imsida, Malta. Mr. Pessia is rated as an Experienced expert by MediFind in the treatment of Megalencephalic Leukoencephalopathy with Subcortical Cysts. He is also highly rated in 2 other conditions, according to our data. His clinical expertise encompasses Drug Induced Dyskinesia, Magnesium Deficiency, Megalencephalic Leukoencephalopathy with Subcortical Cysts, and Astrocytoma.

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    Last Updated: 04/28/2026

    What is the definition of Megalencephalic Leukoencephalopathy with Subcortical Cysts?

    Megalencephalic leukoencephalopathy with subcortical cysts (MLC) is a condition that affects brain development and function. Individuals with this condition have an enlarged brain (megalencephaly) and an abnormality of the white matter in the brain (leukoencephalopathy). White matter consists of nerve fibers covered by a fatty substance called myelin that promotes the rapid transmission of nerve impulses. In MLC, the myelin is swollen and contains numerous fluid-filled pockets (vacuoles). Over time, the swelling decreases and the myelin begins to waste away (atrophy). Leukoencephalopathy can lead to abnormal muscle tensing (spasticity), difficulty coordinating movements (ataxia), cysts in the brain (subcortical cysts), abnormal muscle tone (dystonia), swallowing difficulties, mild to moderate intellectual disabilities, speech difficulties, seizures, and difficulties walking. There are three types of MLC, which are distinguished by their signs and symptoms and genetic cause. Type 1 is caused by genetic changes in the MLC1 gene. Types 2A and 2B are caused by genetic changes in the HEPACAM gene. MLC types 1 and 2A are inherited in an autosomal recessive manner, while type 2B is inherited in an autosomal dominant manner. In some cases of MLC, the cause is unknown.
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