Nonfiction » Health, wellbeing, & medicine » Diseases / genetic

How I Cured My Sick Prostate
Price: $0.99 USD. Words: 1,930. Language: English. Published: September 12, 2020. Categories: Nonfiction » Health, wellbeing, & medicine » Diseases / genetic, Nonfiction » Health, wellbeing, & medicine » herbal medications
According to the medical statistics, about 30% of the men are suffering from this really bad and unpleasant illness - prostatitis. Unfortunately, it possessed me when I was still a boy. My earliest reminiscences date from the primary school. I decided to write this story in order to share all my bad experiences throughout whole my life, until two months ago, when the miracle really happened.
Kidneys Restored to Good Health: Healed From Renal/Kidney Cancer
Price: $18.99 USD. Words: 20,410. Language: English. Published: July 16, 2020. Categories: Nonfiction » Health, wellbeing, & medicine » Diseases / genetic, Nonfiction » Health, wellbeing, & medicine » Diseases / immune system
This healing book restores your kidneys to good health and strengthens your immune system. Prayers send to God Almighty will rise to the Almighty One for your healing flow and he will answer them all. God does not fail. He heals all diseases and life troubles. This amazing Holy Spirit filled book will bring deliverance to your body, sou, mind and life in the Name of Jesus Christ. Enjoy it. Peace!
A new concept of Microchimerism and its Important Role in Autoimmune diseases, Cancer, Wound healing, etc.
Price: $5.00 USD. Words: 3,560. Language: English. Published: May 8, 2020. Categories: Nonfiction » Health, wellbeing, & medicine » Diseases / genetic
An effort has been made in this Booklet to discuss the role of Fetal Microchimerism - a potential contributing factor in wound healing, certain diseases, including cancer etc. along with several relevant illustrations. …Dr. H. K. Saboowala. M.B.(Bom) .M.R.S.H.(London)
Understanding the Impact of Gene mutation on Health & Diseases. An Overview.
Price: $5.00 USD. Words: 5,420. Language: English. Published: April 13, 2020. Categories: Nonfiction » Health, wellbeing, & medicine » Diseases / genetic
Understanding the Impact of Gene mutation on Health & Diseases. An Overview. An attempt has been made in this informative Booklet to summarize the fundamental topics related to genetic mutations and its impact on health and development along with several illustrations. …Dr. H. K. Saboowala. M.B.(Bom) .M.R.S.H.(London)
Fatty Acid Oxidation Disorders, A Simple Guide To The Condition, Diagnosis, Treatment And Related Conditions
Price: $2.99 USD. Words: 10,640. Language: English. Published: December 10, 2019. Categories: Nonfiction » Health, wellbeing, & medicine » Diseases / genetic
This book describes Fatty Acid Oxidation Disorders, Diagnosis and Treatment and Related Diseases Fatty acid oxidation disorders (FODs) are a cluster of genetic metabolic disorders featured by the abnormal breakdown of fatty acids to energy in the body. This process is termed fatty acid oxidation. It is the same as burning fuel in a fireplace but instead of heat the body forms chemical energy.
Fibrodysplasia Ossifican Progressiva (Stone Man Syndrome), A Simple Guide To The Condition, Diagnosis, Treatment And Related Conditions
Price: $2.99 USD. Words: 12,890. Language: English. Published: December 10, 2019. Categories: Nonfiction » Health, wellbeing, & medicine » Diseases / genetic
This book describes Fibrodysplasia Ossifican Progressiva, Diagnosis and Treatment and Related Diseases It is hard to believe that genetic mutations can produce abnormal human illnesses After reading about genetic diseases, I find that there are really such cases found in medical history. Just like the X-men and Incredible Hulk, genetic mutation can produce Stone Man Syndrome and Werewolf Syndrome
CPT Deficiency, A Simple Guide To The Condition, Diagnosis, Treatment And Related Conditions
Price: $2.99 USD. Words: 13,000. Language: English. Published: December 7, 2019. Categories: Nonfiction » Health, wellbeing, & medicine » Diseases / genetic
This book describes CPT Deficiency, Diagnosis and Treatment and Related Diseases Carnitine palmitoyltransferase (CPT) deficiency is a very rare disorder that produces muscle weakness and other symptoms. It happens because of a disease with 1 of 2 enzymes, CPT1 or CPT2 deficient, CPT enzymes help to force fatty acids into cells to usage for energy, CPT deficiency causes muscle and heart weakness
Gaucher Disease, A Simple Guide To The Condition, Diagnosis, Treatment And Related Conditions
Price: $2.99 USD. Words: 14,300. Language: English. Published: December 7, 2019. Categories: Nonfiction » Health, wellbeing, & medicine » Diseases / genetic
This book describes Gaucher Disease, Diagnosis and Treatment and Related Diseases I first came across a rare case of Gaucher Disease in a small boy in Singapore and the parents told me that they are paying U$35,000 for each treatment given. I was shocked by the cost. Gaucher disease is a genetic disorder that cause the abnormal collection of fatty substances called glycolipids in different tissues
Hypertrichosis, (Werewolf syndrome) A Simple Guide To The Condition, Diagnosis, Treatment And Related Conditions
Price: $2.99 USD. Words: 13,000. Language: English. Published: December 7, 2019. Categories: Nonfiction » Health, wellbeing, & medicine » Diseases / genetic
This book describes Hypertrichosis (Werewolf syndrome), Diagnosis and Treatment and Related Diseases While reading about genetic diseases, I came across this disease called hypertrichosis (which means excessive hairs on the body) There was also a story in the Middle Ages of a family with a father Petros Gonzales who look like a wolf man and his normal wife and 2 daughters who were just as hairy
Tuberous Sclerosis, A Simple Guide To The Condition, Diagnosis, Treatment And Related Conditions
Price: $2.99 USD. Words: 19,700. Language: English. Published: November 5, 2019. Categories: Nonfiction » Health, wellbeing, & medicine » Diseases / nervous system (incl. brain), Nonfiction » Health, wellbeing, & medicine » Diseases / genetic
This book describes Tuberous Sclerosis, Diagnosis and Treatment and Related Diseases Tuberous sclerosis complex (TSC) is a genetic disorder that is typically featured by hamartomas in many organs, but especially the skin, brain, eye, kidney and heart. Hamartomas are non-cancerous malformations comprising an overgrowth of the cells and tissues in the affected area and include nevi (birthmarks).
A Simple Guide To Genetic Diseases, Diagnosis, Treatment And Related Conditions
Price: $2.99 USD. Words: 48,040. Language: English. Published: October 20, 2019. Categories: Nonfiction » Health, wellbeing, & medicine » Diseases / genetic
This book describes Genetic Diseases, Diagnosis and Treatment and Related Diseases A genetic disease is a disease produced by an abnormality in the genetic makeup of a person called a mutation. The genetic abnormality can range from minor to major from a single mutation in a single base in the DNA of a single gene to a large chromosomal anomaly such as the addition or subtraction of a chromosome
Fragile X Syndrome, A Simple Guide To The Condition, Diagnosis, Treatment And Related Conditions
Price: $2.99 USD. Words: 14,550. Language: English. Published: October 19, 2019. Categories: Nonfiction » Health, wellbeing, & medicine » Diseases / genetic
This book describes Fragile X Syndrome, Diagnosis and Treatment and Related Diseases Fragile X syndrome (FXS) is a genetic disorder, the second most frequent cause of genetically linked mental deficiencies, after trisomy 21. A genetic disorder indicates that there are alterations to the person’s genes. Fragile X syndrome is the most frequent cause of inherited mental retardation and autism.
Osler’s Disease, A Simple Guide To The Condition, Diagnosis, Treatment And Related Conditions
Price: $2.99 USD. Words: 15,160. Language: English. Published: April 25, 2019. Categories: Nonfiction » Health, wellbeing, & medicine » Diseases / genetic
This book describes Osler’s Disease, Diagnosis and Treatment and Related Diseases Osler disease is an inherited blood vessel disease causing bleeding from the mucous membranes of the nose, gastrointestinal tract, lungs or urinary tract. Patients may also have abnormal blood vessels that bleed in the brain. It is also called Osler-Weber-Rendu syndrome or hereditary hemorrhagic telangiectasis HHT.
Hunter Syndrome, (Mucopolysaccharidosis type II) A Simple Guide To The Condition, Diagnosis, Treatment And Related Conditions
Price: $2.99 USD. Words: 14,260. Language: English. Published: October 4, 2018. Categories: Nonfiction » Health, wellbeing, & medicine » Diseases / genetic, Nonfiction » Health, wellbeing, & medicine » Medicine
This book describes Hunter Syndrome, Diagnosis and Treatment and Related Diseases Hunter syndrome (Mucopolysaccharidosis type II) is a X-linked recessive genetic disorder caused by a missing enzyme. Chains of sugar molecules called glycosaminoglycans collects in organs and brain causing damage. Symptoms Aggressive Hyperactive Brain disability Diagnosis: Genetic test Treatment: Heart Lung symptoms
Polydactyly, (Supernumerary digit) A Simple Guide To The Condition, Diagnosis, Treatment And Related Conditions
Price: $2.99 USD. Words: 10,010. Language: English. Published: September 6, 2018. Categories: Nonfiction » Health, wellbeing, & medicine » Diseases / genetic, Nonfiction » Health, wellbeing, & medicine » Medicine
This book describes Polydactyly, Diagnosis and Treatment and Related Diseases Polydactyly is a congenital disorder where a person has more than 5 fingers per hand Polydactyly may vary from small skin tissues on the hand to fully formed extra fingers with bone, blood vessels and muscle tissue Cause: Genetic Diagnosis: X-ray shows bone in extra digit Treatment: Ligation (skin tissue) Removal (bony)
Hereditary Spherocytosis, A Simple Guide To The Condition, Diagnosis, Treatment And Related Conditions
Price: $2.99 USD. Words: 9,470. Language: English. Published: August 6, 2018. Categories: Nonfiction » Health, wellbeing, & medicine » Medicine, Nonfiction » Health, wellbeing, & medicine » Diseases / genetic
This book describes Hereditary Spherocytosis, Diagnosis and Treatment and Related Diseases Hereditary spherocytosis is a rare disorder of the surface layer of red blood cells, causing red blood cells that look like spheres and breakdown of red blood cells Causes: Genetic Symptoms: Jaundice Anemia Weakness Diagnosis: Spherocytes Reticulocytes Treatment: Splenectomy Folic acid Preventive vaccines
Elephant Man Disease, (Proteus Syndrome) A Simple Guide To The Condition, Diagnosis, Treatment And Related Conditions
Price: $2.99 USD. Words: 12,670. Language: English. Published: July 9, 2018. Categories: Nonfiction » Health, wellbeing, & medicine » Diseases / genetic, Nonfiction » Health, wellbeing, & medicine » Diseases / musculoskeletal
This book describes Elephant Man Disease, Diagnosis and Treatment and Related Diseases Elephant Man Disease is a rare disorder featured by overgrowth of different body tissues caused by a mosaic difference in a gene called AKT1 Proteus syndrome can affect bone, connective tissue, skin, central nervous system and viscera. Treatment Surgery to reduce body overgrowth Blood clot prevention of DVT/PE
Helping Your NF1 Child: A Parent's Guide To Neurofibromatosis
Price: $3.45 USD. Words: 9,350. Language: English. Published: April 12, 2018. Categories: Nonfiction » Health, wellbeing, & medicine » Diseases / genetic, Nonfiction » Health, wellbeing, & medicine » Children’s health
In this short, simple book, Dr. Maloney explains why NF1 varies so widely in how it affects children. For the parents of NF1 children or newly diagnosed adults, Dr. Maloney covers the genetics of NF1 simply. He shows why the disease cannot by predicted by NF1 alone and gives cutting edge research possibilities for its treatment.
Paroxysmal Nocturnal Hemoglobinuria, A Simple Guide To The Condition, Diagnosis, Treatment And Related Conditions
Price: $2.99 USD. Words: 12,540. Language: English. Published: March 11, 2018. Categories: Nonfiction » Health, wellbeing, & medicine » Medicine, Nonfiction » Health, wellbeing, & medicine » Diseases / genetic
This book describes Paroxysmal Nocturnal Hemoglobinuria, Diagnosis and Treatment and Related Diseases Paroxysmal nocturnal hemoglobinuria is a rare genetic disorder in which the red blood cells lining break down faster than normal Diagnosis: Serum hemoglobin/haptoglobin Urine hemosiderin Flow cytometry Treatment: Blood transfusion Eculizumab Vitamin K antagonist Prednisolone Bone marrow transplant
Hemochromatosis, (Iron overload) A Simple Guide To The Condition, Diagnosis, Treatment And Related Conditions
Price: $2.99 USD. Words: 22,730. Language: English. Published: March 11, 2018. Categories: Nonfiction » Health, wellbeing, & medicine » Diseases / genetic, Nonfiction » Health, wellbeing, & medicine » Medicine
This book describes Hemochromatosis, Diagnosis and Treatment and Related Diseases Hemochromatosis (iron overload) is a disease in which too much iron collects in the body Excess iron is toxic, can damage the organs Diagnosis: 1.Transferrin saturation 2.Serum ferritin level 3.Liver function tests. 4.Liver biopsy Treatment: Therapeutic phlebotomy Iron chelation Diet control of iron Liver transplant