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This autosomal dominant disease typically presents in early childhood with a wide clinical spectrum and the development of seizures. GLUT1DS GGM Fanconi-Bickel syndrome T1D

This autosomal dominant disease typically presents in early childhood with a wide clinical spectrum and the development of seizures. GLUT1DS GGM Fanconi-Bickel syndrome T1D

Human Anatomy & Physiology (11th Edition)
Human Anatomy & Physiology (11th Edition)
11th Edition
ISBN:9780134580999
Author:Elaine N. Marieb, Katja N. Hoehn
Publisher:Elaine N. Marieb, Katja N. Hoehn
Chapter1: The Human Body: An Orientation
Section: Chapter Questions
Problem 1RQ: The correct sequence of levels forming the structural hierarchy is A. (a) organ, organ system,...
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Q3: What is the correct answer option, pick one of the choices 

**Question:** This autosomal dominant disease typically presents in early childhood with a wide clinical spectrum and the development of seizures. **Options:** - ⭘ GLUT1DS - ⭘ GGM - ⭘ Fanconi-Bickel syndrome - ⭘ T1D **Explanation:** This question is testing knowledge of genetic disorders. It describes an autosomal dominant disease that presents in early childhood, characterized by a broad range of symptoms and the occurrence of seizures. Understanding the genetic basis and clinical features is crucial for diagnosing and managing these conditions.
Transcribed Image Text:**Question:** This autosomal dominant disease typically presents in early childhood with a wide clinical spectrum and the development of seizures. **Options:** - ⭘ GLUT1DS - ⭘ GGM - ⭘ Fanconi-Bickel syndrome - ⭘ T1D **Explanation:** This question is testing knowledge of genetic disorders. It describes an autosomal dominant disease that presents in early childhood, characterized by a broad range of symptoms and the occurrence of seizures. Understanding the genetic basis and clinical features is crucial for diagnosing and managing these conditions.
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