Journal Article

Clinical spectrum of MTOR-related hypomelanosis of Ito with neurodevelopmental abnormalities

Amram, Daniel, Aubriot-Lorton, Marie-Hélène, Philippe, Christophe, Sorlin, Arthur, Goujon, Louise, Jacquemont, Marie-Line, Chevarin, Martin, Semple, Robert K., Rodriguez, Diana, Olaso, Robert, Deleuze, Jean-François, Boland, Anne, Rollier, Paul, Parker, Victoria E.R., Grotto, Sarah, Carmignac, Virginie, Vabres, Pierre, Fraitag, Sylvie, Polubothu, Satyamaanasa, Quelin, Chloé, Mignot, Cyril, Arzimanoglou, Alexis, Kuentz, Paul, Knox, Rachel G., Rivière, Jean-Baptiste, Guibaud, Laurent, Courcet, Jean-Benoît, Geneviève, David, Delepine, Marc, Darmency, Véronique, Odent, Sylvie, Capri, Yline, Faivre, Laurence, Blanchard, Emmanuelle, Duffourd, Yannis, Sarret, Catherine, Bessis, Didier, Riachi, Melissa, Keddar, Malika, Callier, Patrick, Thauvin, Christel, Kinsler, Veronica A., Vincent-Delorme, Catherine, Catteau, Benoît

2021

Overview

Hypomelanosis of Ito (HI) is a skin marker of somatic mosaicism. Mosaic MTOR pathogenic variants have been reported in HI with brain overgrowth. We sought to delineate further the pigmentary skin phenotype and clinical spectrum of neurodevelopmental manifestations of MTOR-related HI. From two cohorts totaling 71 patients with pigmentary mosaicism, we identified 14 patients with Blaschko-linear and one with flag-like pigmentation abnormalities, psychomotor impairment or seizures, and a postzygotic MTOR variant in skin. Patient records, including brain magnetic resonance image (MRI) were reviewed. Immunostaining (n = 3) for melanocyte markers and ultrastructural studies (n = 2) were performed on skin biopsies. MTOR variants were present in skin, but absent from blood in half of cases. In a patient (p.[Glu2419Lys] variant), phosphorylation of p70S6K was constitutively increased. In hypopigmented skin of two patients, we found a decrease in stage 4 melanosomes in melanocytes and keratinocytes. Most patients (80%) had macrocephaly or (hemi)megalencephaly on MRI. MTOR-related HI is a recognizable neurocutaneous phenotype of patterned dyspigmentation, epilepsy, intellectual deficiency, and brain overgrowth, and a distinct subtype of hypomelanosis related to somatic mosaicism. Hypopigmentation may be due to a defect in melanogenesis, through mTORC1 activation, similar to hypochromic patches in tuberous sclerosis complex. [Display omitted]

• Publisher: Elsevier Inc,Nature Publishing Group US,Nature Publishing Group
• Subject: Biomedical and Life Sciences / Biomedicine / Genetics / Human Genetics / Humans / Hypopigmentation - genetics / Laboratory Medicine / Life Sciences / Mechanistic Target of Rapamycin Complex 1 - genetics / Megalencephaly / Mosaicism / Neurons and Cognition / Phenotype / TOR Serine-Threonine Kinases - genetics