Modern Medicine in Digital format

The most modern format of medicine of the Digital World

The frequencies used in these Modern Medicine in Digital format are based upon single frequency or combo of frequencies used in Rife sets and are masked in Algorithmic piano music.

More details regarding the Chromosome Abnormalities is given the list below is given below the list.

List of Modern Medicine in Digital format for Chromosome Abnormalities available at us for just Rs. 500/- for any 5 sessions from given below for 30 doses per session (2 times a day for 15 days) in max 15 days.

1) Chromosome-5p Syndrome
2)  Chromosome 16 Abnormalities
3)  Chromosome 17 Abnormalities
4)  Chromosome 18 Abnormalities
5)  Chromosome 20 Abnormalities
6)  Chromosome 22 Abnormalities

Details regarding the Chromosome Abnormalities Related Disorders related List above

* Human Chromosome 5p deletion syndrome. Cri-du-chat syndrome is caused by a deletion of the end of the short (p) arm of chromosome 5. This chromosomal change is written as 5p-. The signs and symptoms of cri-du-chat syndrome are probably related to the loss of multiple genes in this region. Researchers have not identified all of these genes or determined how their loss leads to the features of the disorder. They have discovered, however, that a larger deletion tends to result in more severe mental retardation and developmental delays in people with cri-du-chat syndrome. Researchers have defined narrow regions of the short arm of chromosome 5 that are associated with particular features of cri-du-chat syndrome. A specific region designated 5p15.3 is associated with a cat-like cry, and a nearby region called 5p15.2 is associated with mental retardation, small head (microcephaly), and distinctive facial features.

* Human Chromosome 16, Trisomy 16, Familial Mediterranean fever (FMF), Crohn's disease, Thalassemia, Autosomal dominant polycystic kidney disease (PKD-1), Autism, Schizophrenia, Obesity?

* Human Chromosome 17, 17Q21.31 Microdeletion Syndrome, Alexander disease, Andersen-Tawil syndrome, Birt-Hogg-Dube syndrome, Bladder cancer, Breast cancer, Camptomelic dysplasia, Canavan disease, Cerebroretinal microangiopathy with calcifications and cysts, Charcot-Marie-Tooth disease, Charcot-Marie-Tooth disease -type 1, Corticobasal degeneration, Cystinosis, Depression, Ehlers-Danlos syndrome, Ehlers-Danlos syndrome, arthrochalasia type, Ehlers-Danlos syndrome, classical type, Epidermodysplasia verruciformis, Galactosemia, Glycogen storage disease type II (Pompe disease), Hereditary neuropathy with liability to pressure palsies, Howel-Evans syndrome, Li-Fraumeni syndrome, Maturity onset diabetes of the young type 5, Miller-Dieker syndrome, Multiple synostoses syndrome, Neurofibromatosis -type I, Nonsyndromic deafness, Nonsyndromic deafness, autosomal dominant, Nonsyndromic deafness, autosomal recessive, Osteogenesis imperfecta, Osteogenesis Imperfecta -type I, Osteogenesis Imperfecta -type II, Osteogenesis Imperfecta -type III, Osteogenesis Imperfecta -type IV, Proximal symphalangism, Smith-Magenis syndrome, Usher syndrome, Usher syndrome -type I, Very long-chain acyl-coenzyme A dehydrogenase deficiency.

* Human Chromosome 18, Erythropoietic Protoporphyria, Hereditary Hemorrhagic Telangiectasia, Niemann-Pick disease Type C, Porphyria, Selective Mutism, Edwards syndrome (Trisomy 18), Tetrasomy 18p, Monosomy 18p, Pitt Hopkins Syndrome 18q21.

* Human Chromosome 20, Albright's hereditary osteodystrophy, Arterial tortuosity syndrome, Adenosine deaminase deficiency, Alagille syndrome, Celiac disease, Galactosialidosis - CTSA, Maturity onset diabetes of the young type 1, Neuronal ceroid lipofuscinosis, Pantothenate kinase-associated neurodegeneration, Transmissible spongiform encephalopathy (prion diseases), Waardenburg syndrome.

* Human Chromosome 22, Amyotrophic lateral sclerosis, Breast cancer, DiGeorge Syndrome, Desmoplastic small round cell tumor, 22q11.2 deletion syndrome, 22q13 deletion syndrome or Phelan-McDermid syndrome, Li-Fraumeni syndrome, Neurofibromatosis type 2, Rubinstein-Taybi syndrome, Waardenburg syndrome, Cat eye syndrome, Methemoglobinemia, Schizophrenia, Male-pattern baldness? Cat-eye Syndrome, Emanuel Syndrome, Leukemia. Other changes in the number or structure of chromosome 22 can have a variety of effects, including mental retardation, delayed development, physical abnormalities, and other medical problems.