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Pigmentation abnormalities in Coffin-Siris syndrome.
Eugenio Zapata-Aldana1, Delia Ceballos-Sáenz1, Jorge Rodrigo Vásquez-Ríos1
1Telethon's Children's Rehabilitation Centre (Centro de Rehabilitación e Inclusión Infantil Teletón), Guerrero, Mexico.
Pigmentary abnormalities are a key feature of Coffin-Siris Syndrome, highlighting the condition's diverse presentation. Recognizing these skin findings is crucial for accurate diagnosis and understanding the full spectrum of Coffin-Siris Syndrome patient phenotypes.
Area of Science:
- Genetics
- Dermatology
- Rare Diseases
Background:
- Coffin-Siris Syndrome (CSS) is a rare genetic disorder characterized by distinctive facial features, developmental delay, and growth retardation.
- Ocular and skin findings are frequently reported in CSS, but pigmentary abnormalities are often overlooked.
- Understanding the full phenotypic spectrum is essential for comprehensive patient management.
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