Create a scientific poster summary graphic based on a case report of Marfan syndrome with X trisomy and FBN1 and SDHB mutations. The central figure should represent a patient with clear callouts for key genetic findings: FBN1 mutation, SDHB mutation, and X trisomy. Include main clinical features such as myopia, connective tissue disorder, and risk of tumors. Also show treatment and prognosis details including posterior scleral reinforcement and improved visual acuity. Use a clean, professional style with a solid white background and bold black text for all labels. The design should be suitable for medical professionals and students. Reference the provided case report image for context. emoji | AI Emoji Generator
Attribute this emoji
Remember to mention the source when using this image. Copy the attribution details below and include them on your project.
No spells required — Go premium and make attribution disappear
Create a scientific poster summary graphic based on a case report of Marfan syndrome with X trisomy and FBN1 and SDHB mutations. The central figure should represent a patient with clear callouts for key genetic findings: FBN1 mutation, SDHB mutation, and X trisomy. Include main clinical features such as myopia, connective tissue disorder, and risk of tumors. Also show treatment and prognosis details including posterior scleral reinforcement and improved visual acuity. Use a clean, professional style with a solid white background and bold black text for all labels. The design should be suitable for medical professionals and students. Reference the provided case report image for context.emoji
Model
Solid
Date
May 29, 2025
Attribute this emoji
Remember to mention the source when using this image. Copy the attribution details below and include them on your project.
No spells required — Go premium and make attribution disappear
Create a scientific poster summary graphic based on a case report of Marfan syndrome with X trisomy and FBN1 and SDHB mutations. The central figure should represent a patient with clear callouts for key genetic findings: FBN1 mutation, SDHB mutation, and X trisomy. Include main clinical features such as myopia, connective tissue disorder, and risk of tumors. Also show treatment and prognosis details including posterior scleral reinforcement and improved visual acuity. Use a clean, professional style with a solid white background and bold black text for all labels. The design should be suitable for medical professionals and students. Reference the provided case report image for context.emoji