Hereditary Genetics: Current Research

Hereditary Genetics Current Research is a peer reviewed scientific, open access journal known for rapid dissemination of high-quality research.

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#Psychiatric genetics is a subfield of behavioral neurogenetics and behavioral genetics which studies the role of #genetics in the development of mental disorders.
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#Genetic variation within a population is commonly measured as the percentage of #polymorphic gene loci or the percentage of gene loci in heterozygous individuals.
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#Feingold syndrome is an #autosomal dominant disorder characterized by variable combinations of microcephaly, limb malformations, esophageal and duodenal atresias, and learning disability/mental retardation.
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#FG syndrome type 1 is an #X-linked genetic disorder that is characterized by poor muscle tone , intellectual disability, constipation and or anal anomalies.
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[Hereditary Genetics: Current Research @CurrentGenetics]

#Joubert syndrome is a #rare genetic condition characterized by abnormal brain development that includes the absence or underdevelopment of the cerebellar vermis and a malformed brain stem.
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#Kniest dysplasia happens because of a #gene change. The changed gene causes a problem with the growth plate of the bone, which leads to abnormal bone growth and shape.
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#Kufor Rakeb syndrome (KRS), also known as #Parkinson's disease 9, is a very rare form of inherited juvenile-onset Parkinson's disease.
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#Li-Fraumeni syndrome is a rare #hereditary or genetic disorder that increases the risk you and your family members will develop cancer.
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#Overgrowth syndromes are caused by #gene mutations or abnormalities. The exact genetic cause is sometimes unknown.
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#Krabbe disease is a rare, #inherited metabolic disorder in which harmful amounts of lipids (fatty materials such as oils and waxes) build up in various cells and tissues in the body and destroy brain cells.
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[Hereditary Genetics: Current Research @CurrentGenetics]

#Kufor Rakeb syndrome (KRS), also known as Parkinson's disease 9, is a very rare form of #inherited juvenile-onset Parkinson's disease.
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#Lesch-Nyhan syndrome (LNS) is a rare, #inherited disorder caused by a deficiency of the enzyme hypoxanthine-guanine phosphoribosyltransferase (HPRT).
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#Li-Fraumeni syndrome is a rare #hereditary or genetic disorder that increases the risk you and your family members will develop cancer.
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#Lynch syndrome is a type of #inherited cancer syndrome associated with a genetic predisposition to different cancer types.
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#Maroteaux-Lamy syndrome is a rare #genetic disorder characterized by complete or partial lack of activity of the enzyme arylsulfatase B, encoded by the ARSB gene.
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McCune-Albright syndrome is a genetic condition that affects your bones, skin and endocrine system, causing skin pigmentation, scar tissue forming on bones and irregular function of growth-regulating glands that produce hormones.
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#McLeod neuroacanthocytosis syndrome is primarily a #neurological disorder that occurs almost exclusively in boys and men.
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#Familial Mediterranean fever (FMF) is an #autoinflammatory genetic disorder that mainly affects people of Mediterranean origin.
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#Methemoglobinemia (MetHb) is a #blood disorder in which an abnormal amount of methemoglobin is produced.
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#Micro syndrome is an #autosomal recessive disorder caracterised by ocular and neurodevelopmental defects and by microgenitalia.
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