# Atrophic, translucent plaque on the scalp of a newborn

**Authors:** Racquel A. Bitar, Sarah E. Servattalab, Yasin Damji

PMC · DOI: 10.1016/j.jdcr.2025.09.022 · 2025-10-10

## Full-text entities

- **Genes:** NOTCH3 (notch receptor 3) [NCBI Gene 4854] {aka CADASIL, CADASIL1, CARASIL1, CASIL, FPLD1, IMF2}
- **Diseases:** intrauterine infection (MESH:D007239), dermatologic condition (MESH:D000168), melanocytosis (MESH:C535835), congenital hemangioma (MESH:D006391), embryological malformations (MESH:C564254), dermal pigment incontinence (MESH:D014549), Epidermal nevus (MESH:C580062), ACC (MESH:D004476), placental infarctions (MESH:D007238), Nevus sebaceus (MESH:D054000), pre-eclampsia (MESH:D011225), intrauterine growth restriction (MESH:D005317), Congenital melanocytic nevus (MESH:C536819), dermal fibrosis (MESH:D005355), central nervous system or bone defects (MESH:D009421), trauma (MESH:D014947), gestational diabetes (MESH:D016640), alopecia (MESH:D000505)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12648715/full.md

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Source: https://tomesphere.com/paper/PMC12648715