Rare Disease from A to Z
Did you know there are over 7,000 known rare diseases? Follow our narrator, Effie, as she uses the alphabet to explain 26 rare diseases in a scientifically accurate, but easy to understand, way.

Featured rare diseases include: Aicardi Syndrome, Baraitser Winter Syndrome, CDKL5 Deficiency Disorder, Desanto-Shinawi Syndrome, Ectodermal Dysplasia, FOXG1 Syndrome, Glycogen storage disease, Hemimegalencephaly, Infantile Bullous Pemphigoid, Joubert Syndrome, Kabuki Syndrome, Leukodystrophy/Leuden Syndrome, Moebius Syndrome, Non-ketotic hyperglycinemia, Osteogenesis Imperfecta, Prader Willi Syndrome, 22Q13- Phelan McDermid Syndrome, Russell Silver Syndrome, Sanfilippo Syndrome, Tuberous Sclerosis Complex, undiagnosed, Vein of Galen Malformation, Wolf Hirschhorn Syndrome, Xia-Gibbs Syndrome, PYROXD-1, and Zimmerman Laband syndrome.

"Rare Disease from A to Z" is the second book in the series by Simply Complex Stories. By presenting medical diagnoses and disabilities in a relatable but accurate way, Simply Complex Stories equips children (and adults) with empathy and understanding, fostering a more inclusive world. Learn more at simplycomplexstories.com or by following along on Instagram at @simplycomplexstories
1146501287
Rare Disease from A to Z
Did you know there are over 7,000 known rare diseases? Follow our narrator, Effie, as she uses the alphabet to explain 26 rare diseases in a scientifically accurate, but easy to understand, way.

Featured rare diseases include: Aicardi Syndrome, Baraitser Winter Syndrome, CDKL5 Deficiency Disorder, Desanto-Shinawi Syndrome, Ectodermal Dysplasia, FOXG1 Syndrome, Glycogen storage disease, Hemimegalencephaly, Infantile Bullous Pemphigoid, Joubert Syndrome, Kabuki Syndrome, Leukodystrophy/Leuden Syndrome, Moebius Syndrome, Non-ketotic hyperglycinemia, Osteogenesis Imperfecta, Prader Willi Syndrome, 22Q13- Phelan McDermid Syndrome, Russell Silver Syndrome, Sanfilippo Syndrome, Tuberous Sclerosis Complex, undiagnosed, Vein of Galen Malformation, Wolf Hirschhorn Syndrome, Xia-Gibbs Syndrome, PYROXD-1, and Zimmerman Laband syndrome.

"Rare Disease from A to Z" is the second book in the series by Simply Complex Stories. By presenting medical diagnoses and disabilities in a relatable but accurate way, Simply Complex Stories equips children (and adults) with empathy and understanding, fostering a more inclusive world. Learn more at simplycomplexstories.com or by following along on Instagram at @simplycomplexstories
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Rare Disease from A to Z

Rare Disease from A to Z

Rare Disease from A to Z

Rare Disease from A to Z

Overview

Did you know there are over 7,000 known rare diseases? Follow our narrator, Effie, as she uses the alphabet to explain 26 rare diseases in a scientifically accurate, but easy to understand, way.

Featured rare diseases include: Aicardi Syndrome, Baraitser Winter Syndrome, CDKL5 Deficiency Disorder, Desanto-Shinawi Syndrome, Ectodermal Dysplasia, FOXG1 Syndrome, Glycogen storage disease, Hemimegalencephaly, Infantile Bullous Pemphigoid, Joubert Syndrome, Kabuki Syndrome, Leukodystrophy/Leuden Syndrome, Moebius Syndrome, Non-ketotic hyperglycinemia, Osteogenesis Imperfecta, Prader Willi Syndrome, 22Q13- Phelan McDermid Syndrome, Russell Silver Syndrome, Sanfilippo Syndrome, Tuberous Sclerosis Complex, undiagnosed, Vein of Galen Malformation, Wolf Hirschhorn Syndrome, Xia-Gibbs Syndrome, PYROXD-1, and Zimmerman Laband syndrome.

"Rare Disease from A to Z" is the second book in the series by Simply Complex Stories. By presenting medical diagnoses and disabilities in a relatable but accurate way, Simply Complex Stories equips children (and adults) with empathy and understanding, fostering a more inclusive world. Learn more at simplycomplexstories.com or by following along on Instagram at @simplycomplexstories

Product Details

ISBN-13: 9798218514952
Publisher: Simply Complex Stories
Publication date: 10/04/2024
Series: Simply Complex Stories
Pages: 50
Product dimensions: 8.50(w) x 8.50(h) x 0.13(d)
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