Cystic fibrosis is an autosomal recessive (inherited) disorder - the genetic mutation 🧬 causes excessive amounts of thick, sticky mucus throughout the body. This mucus can cause blockages ⛔ in areas of the body such as the bronchi, small intestines, and pancreatic and bile ducts. And when this mucus plugs up the bronchi, it causes lots of respiratory problems ⚠️ for our clients! 📌 Save these cystic fibrosis quick tips for your nursing school and NGN studying! 🙌 #futurenurse #newgradnurse #nur
1:28
FacebookArcher NCLEX Review
Cystic fibrosis is an autosomal recessive (inherited) disorder - the genetic mutation 🧬 causes excessive amounts of thick, sticky mucus throughout the body. This mucus can cause
Archer NCLEX Review. . Cystic fibrosis is an autosomal recessive (inherited) disorder - the genetic mutation 🧬 causes excessive amounts of thick, sticky mucus throughout the body. This mucus can cause blockages ⛔ in areas of the body such as the bronchi, small intestines, and pancreatic and bile ducts. And when this mucus plugs up the ...
4K views11 months ago
Genetic Disorders Explained
Genetic Mutations & Disorders Explained: A High School Guide with Examples This instructional video breaks down the fundamentals of genetic mutations and related disorders for high school students. Using clear diagrams and real-world examples like sickle cell anemia and cystic fibrosis, it explains how mutations occur and their impact on health. The content is designed to make complex genetic concepts easy to understand and engaging. Perfect for classroom learning or self-study on YouTube and ed
2:50
Genetic Mutations & Disorders Explained: A High School Guide with Examples This instructional video breaks down the fundamentals of genetic mutations and related disorders for high school students. Using clear diagrams and real-world examples like sickle cell anemia and cystic fibrosis, it explains how mutations occur and their impact on health. The content is designed to make complex genetic concepts easy to understand and engaging. Perfect for classroom learning or self-study on YouTube and ed
FacebookFilipino Science Hub
10.4K views3 months ago
Genetic Disorders Explained 🧬 | 'Copy-Paste' Error in DNA | Class 12 Biology | UP Board RWA
47:54
Genetic Disorders Explained 🧬 | 'Copy-Paste' Error in DNA | Class 12 Biology | UP Board RWA
YouTubeUP Board English Medium
525 views2 weeks ago
Piebaldism Explained: The Gene Behind the White Hair Streak
0:47
Piebaldism Explained: The Gene Behind the White Hair Streak
YouTubeDoctor Sood
31.3K views1 week ago
Top videos
Everything you Need to Know:Chromosome Analysis (Karyotyping)
2:22
Everything you Need to Know:Chromosome Analysis (Karyotyping)
YouTubeAl Borg Diagnostics
163.2K viewsMay 21, 2019
Neurofibromatosis is a genetic disorder that causes tumors to grow along nerves in the body, skin, and brain. These tumors are usually noncancerous, but they can lead to skin changes, bone deformities, hearing or vision problems, and learning difficulties depending on their size and location. There are three main types - NF1, NF2, and schwannomatosis - each with different symptoms and severity. The condition is inherited in most cases, though it can also occur through random genetic mutation. |
Neurofibromatosis is a genetic disorder that causes tumors to grow along nerves in the body, skin, and brain. These tumors are usually noncancerous, but they can lead to skin changes, bone deformities, hearing or vision problems, and learning difficulties depending on their size and location. There are three main types - NF1, NF2, and schwannomatosis - each with different symptoms and severity. The condition is inherited in most cases, though it can also occur through random genetic mutation. |
FacebookO23 EcoTech
1.5K views2 weeks ago
CDKL5 deficiency disorder (CDD) is a genetic condition that causes seizures and significant delays in many aspects of development. CDD is about #MoreThanSeizures, it’s about daily challenges and interruptions to family life, it’s about skipping lunch to provide care. On World #CDKL5 Day, hear from Karen Utley, President & Co-Founder, International Foundation for CDKL5 Research, about her experiences. #CDKL5awareness | UCB Biopharma
1:09
CDKL5 deficiency disorder (CDD) is a genetic condition that causes seizures and significant delays in many aspects of development. CDD is about #MoreThanSeizures, it’s about daily challenges and interruptions to family life, it’s about skipping lunch to provide care. On World #CDKL5 Day, hear from Karen Utley, President & Co-Founder, International Foundation for CDKL5 Research, about her experiences. #CDKL5awareness | UCB Biopharma
FacebookUCB Biopharma
726K views3 months ago
Rare Genetic Disorders
Rare Genetic Diseases
Rare Genetic Diseases
genome.gov
Apr 13, 2018
10 Rare Genetic Cat Diseases - Canine Journal
2:54
10 Rare Genetic Cat Diseases - Canine Journal
caninejournal.com
Jul 30, 2018
Genetic and Rare Diseases Information Center
Genetic and Rare Diseases Information Center
genome.gov
10 months ago
Everything you Need to Know:Chromosome Analysis (Karyotyping)
2:22
Everything you Need to Know:Chromosome Analysis (Kar…
163.2K viewsMay 21, 2019
YouTubeAl Borg Diagnostics
Neurofibromatosis is a genetic disorder that causes tumors to grow along nerves in the body, skin, and brain. These tumors are usually noncancerous, but they can lead to skin changes, bone deformities, hearing or vision problems, and learning difficulties depending on their size and location. There are three main types - NF1, NF2, and schwannomatosis - each with different symptoms and severity. The condition is inherited in most cases, though it can also occur through random genetic mutation. |
Neurofibromatosis is a genetic disorder that causes tumors to gr…
1.5K views2 weeks ago
FacebookO23 EcoTech
CDKL5 deficiency disorder (CDD) is a genetic condition that causes seizures and significant delays in many aspects of development. CDD is about #MoreThanSeizures, it’s about daily challenges and interruptions to family life, it’s about skipping lunch to provide care. On World #CDKL5 Day, hear from Karen Utley, President & Co-Founder, International Foundation for CDKL5 Research, about her experiences. #CDKL5awareness | UCB Biopharma
1:09
CDKL5 deficiency disorder (CDD) is a genetic condition that causes se…
726K views3 months ago
FacebookUCB Biopharma
Sickle Cell Anemia | A Genetic Disorder | Lecture 12
10:29
Sickle Cell Anemia | A Genetic Disorder | Lecture 12
117.2K viewsApr 22, 2022
YouTubePoWer Of KnOwledge Academy
Introduction to Genetic Disorders ✨
4:37
Introduction to Genetic Disorders ✨
27.4K viewsOct 29, 2021
YouTubeNonsense Mutation Foundation
Primary mitochondrial myopathy - causes, symptoms, diagnosis, treatment, pathology
5:41
Primary mitochondrial myopathy - causes, symptoms, diagnosis, tre…
68.4K viewsJan 15, 2020
YouTubeOsmosis from Elsevier
Knox County student Kennedy Welch has Familial Hypercholesterolemia, a genetic disorder that causes high cholesterol levels from birth. She shares her journey with FH and why it's important for children to get tested at a young age. | Knox County Health Department
Knox County student Kennedy Welch has Familial Hypercholeste…
289 views2 weeks ago
FacebookKnox County Health Department
4:41
How this disease changes the shape of your cells - Amber M. Yates
1.4M viewsMay 6, 2019
YouTubeTED-Ed
3:59
Sickle Cell Anemia
1.3M viewsOct 4, 2022
YouTubeNucleus Medical Media
7:17
Beta-thalassemia - causes, symptoms, diagnosis, treatment, …
407.1K viewsOct 11, 2022
YouTubeOsmosis from Elsevier
7:10
Down's Syndrome | A Genetic Disorder | Lecture 13
211.8K viewsApr 22, 2022
YouTubePoWer Of KnOwledge Academy
4:59
Edwards Syndrome, Causes, Signs and Symptoms, Diagnosis and Tre…
68.8K viewsNov 12, 2021
YouTubeMedical Centric
6:54
Marfan Syndrome - causes, symptoms, diagnosis, treatment, …
475.7K viewsOct 30, 2017
YouTubeOsmosis from Elsevier
6:15
PhenylKetonuria (PKU) | A Genetic Disorder | Lecture 14
66.4K viewsApr 23, 2022
YouTubePoWer Of KnOwledge Academy
24:56
Sickle Cell Anemia Nursing | Symptoms, Pathophysiology, Sick…
771.2K viewsMay 12, 2018
YouTubeRegisteredNurseRN
1:58
2-Minute Neuroscience: Amyotrophic Lateral Sclerosis (ALS)
407.5K viewsMar 14, 2017
YouTubeNeuroscientifically Challenged
4:09
Inherited Genetic Disorders | Genetics | Biology | FuseSchool
336.2K viewsJun 18, 2019
YouTubeFuseSchool - Global Education
What is Bloom Syndrome? | Genetic Disorder | Causes And Symptoms …
390 views1 month ago
YouTubeThe Study IAS By Manikant Singh
4:43
Baby with Epidermolysis Bullosa | Rare Genetic Skin Disorder Explai…
4.7K views1 month ago
YouTubeDr Shehzad paediatrician
1:59
2-Minute Neuroscience: Huntington's disease
312.5K viewsJul 6, 2018
YouTubeNeuroscientifically Challenged
1:06
[WATCH] Mahlatse Marema (15) from Randfontein, who has neurof…
31.4K views1 month ago
FacebookNewzroom Afrika
2:27
194K views · 2.4K reactions | WATCH: Second oldest in the worl…
194K views3 weeks ago
FacebookGlobal Toronto
11:08
2.4M views · 53K reactions | Nathan and Bennett are both diagnosed w…
2.4M views3 weeks ago
FacebookSpecial Books by Special Kids
1:13
What Causes GAD? Genetics, Temperament, Stress & the Biops…
619 views3 weeks ago
YouTubeDr. Mike Mah
1:58
Libbie's story: Larsen syndrome, …
NATIONALLY RATED HOSPITAL
About this channel
YouTubeChildren's Wisconsin
4:44
Haemophilia, Causes, SIgns and Symptoms, Diagnosis and Treatm…
116.2K viewsApr 15, 2021
YouTubeMedical Centric
5:32
PRADER WILLI SYNDROME(PWDS), Causes, Signs and Symptoms, Dia…
72.5K viewsMay 21, 2019
YouTubeMedical Centric
Explaining on Instagram: "Follow (us) @Explaining to learn somethi…
1.6M views3 weeks ago
Instagramexplaining
4:20
What Is Sickle Cell Anemia and How Do You Get It?
210.1K viewsFeb 27, 2018
YouTubeSeeker
See more videos
Static thumbnail place holder