Several deficiencies
-
Objectives: (1) Determine the proportions of hypoalbuminemia and iron deficiency anemia in children aged from 2 months to under 5 years old with pneumonia at Ca Mau Obstetrics and Pediatrics Hospital in 2022-2023 (2) Evaluate the association between hypoalbuminemia, iron deficiency anemia and pneumonia in children aged from 2 months to under 5 years old at Ca Mau Obstetrics and Pediatrics Hospital in 2022-2023.
7p vikoch 27-06-2024 1 1 Download
-
Mutation of the IL2RG gene results in a form of severe combined immune deficiency (SCID-X1), which has been treated successfully with hematopoietic stem cell gene therapy. SCID-X1 gene therapy results in reconstitution of the previously lacking T cell compartment, allowing analysis of the roles of T cell immunity in humans by comparing before and after gene correction.
14p vibransone 28-03-2024 7 2 Download
-
Ebook "Reelin glycoprotein: Structure, biology and roles in health and disease" is a serine protease with important roles in embryogenesis and during adult life. Reelin mutations or deficiency of the protein product could cause abnormal cortical development and reelin signaling impairment in brain. Reelin abnormalities in several neurospychiatric disorders, such as autism, schizophrenia, mood disorders and lissencephaly, may provide mechanistic explanations for etiologies of these disorders.
473p cotieubac1004 15-03-2024 2 0 Download
-
Recurrent episodes of hypoglycemia may be caused by several factors, including drugs, critical illnesses, hormonal defciency, non-islet cell tumor endogenous hyperinsulinism, and accidental, surreptitious, or malicious hypoglycemia. Multiple drugs have been previously reported as causes of hypoglycemia, with moderate and lowquality evidence.
4p vitiki 30-01-2024 3 2 Download
-
Factor XII deficiency can be related to either homozygous or compound heterozygous pathogenic variants in the F12 gene. The disease is commonly known as Hageman trait and is inherited in both autosomal recessive or dominant patterns.
4p vitiki 30-01-2024 4 2 Download
-
Part 1 book "Case studies in veterinary immuneology" includes content: Primary ciliary dyskinesia—canine; leukocyte adhesion deficiency—bovine; cyclic neutropenia—canine; chediak–higashi syndrome—feline; severe combined immunodeficiency—equine; selective iga deficiency—canine; failure of passive transfer—equine; feline leukemia virus—feline; feline immunodeficiency virus—feline; bovine viral diarrhea virus—bovine; marek’s disease—avian; infectious bursal disease—avian,... and other contents.
100p muasambanhan05 16-01-2024 3 0 Download
-
Vitamin B12 deficiency is a well-known cause of anemia. Pancytopenia and hemolysis are less frequently observed in vitamin B12 deficiency. Reported is the case of a 58-year-old man who presented with dyspnea on exertion, fatigue, and unintentional weight loss.
3p viintuit 26-09-2023 2 0 Download
-
Merosin-deficient congenital muscular dystrophy (MDCMD) is a progressive autosomal recessive disorder caused by the lack of expression of the α2-chain of laminin-211 glycoprotein. The defect results in skeletal muscle dysfunction with severe muscle weakness, hypotonia, proximal joint contractures, facial dysmorphism, and late or failed ambulation.
5p viintuit 26-09-2023 0 0 Download
-
Leukocyte adhesion deficiency type 1 (LAD1) is a rare congenital immunodeficiency disease. The cause of disease is determined to be the mutations in the ITGB2 gene that codes for CD18, the beta chain of beta-2 integrins, leads to decreased expression or functioning of CD18. This deficiency leads to severe impairment of leukocyte adhesion to the vascular wall and leukocyte migration to sites of infection and inflammation.
7p vimulcahy 18-09-2023 5 3 Download
-
Hereditary folate malabsorption—a rare disorder caused by impairment of the folate transporter—can develop into severe folate deficiency manifesting as megaloblastic anemia and occasionally thrombocytopenia. Reportedly, megaloblastic anemia can manifest with hemorrhagic episodes, possibly due to ineffective platelet production and platelet dysfunction.
6p vigamora 23-05-2023 5 2 Download
-
One of the most common types of congenital adrenal hyperplasia is an autosomal recessive disorder with 21-hydroxylase deficiency. The classical form, defined by cortisol insufficiency, is accompanied by prenatal androgen excess causing variable masculinization degrees of external genitalia in babies with a 46, XX karyotype.
6p vigamora 23-05-2023 5 2 Download
-
Denosumab is known to cause abnormalities in calcium homeostasis. Most of such cases have been described in patients with underlying chronic kidney disease or severe vitamin D deficiency. Previous bariatric surgery could also contribute to hypocalcemia and deterioration in bone health.
5p videadpool 05-05-2023 2 2 Download
-
The research article "Polyester production by halophilic and halotolerant bacterial strains obtained from mangrove soil samples located in Northern Vietnam" reports halophilic and halotolerant bacteria isolated from mangrove forests located in Northern Vietnam. Several of these bacteria were able to synthesize polyhydroxyalkanoates (PHAs). PHAs are polyesters stored by microorganisms under the presence of considerable amounts of a carbon source and deficiency of other essential nutrient such as nitrogen or phosphorous.
12p runordie3 27-06-2022 10 3 Download
-
The content of this article opens the research directions related to climate change and adaption of resident as well as the government under its impacts on human health and socio-economic life in the Ho Chi Minh City areas. In particular, this study offers a unifying conceptual framework for capturing and studying the interlinkages between climate change and the livelihood of the urban poor.
14p visherylsandberg 18-05-2022 10 1 Download
-
Magnesium is the second most abundant intracellular cation and a co-factor in several reactions involved in the formation and usage of adenosine triphosphate and nucleic acid synthesis. Magnesium deficiency may be as high as 65 % in patients admitted to a medical Intensive Care Unit (ICU).
8p viisaacnewton 25-04-2022 8 1 Download
-
A strain of Leghorn chickens (rd/rd), unable to produce a functional riboflavin-binding protein, lays riboflavin-deficient eggs, in which all embryos suddenly die at mid-incubation (days 13-15). This malady, caused by riboflavin deficiency, leads to excessive lipid accumulation in liver, impaired β-oxidation of lipid, and severe hypoglycemia prior to death.
30p vibeauty 23-10-2021 12 0 Download
-
Nuclear reprogramming reinstates totipotency or pluripotency in somatic cells by changing their gene transcription profile. This technology is widely used in medicine, animal husbandry and other industries. However, certain deficiencies severely restrict the applications of this technology
15p vitzuyu2711 29-09-2021 4 1 Download
-
‘Candidatus Phytoplasma solani’ is endemic in Europe and infects a wide range of weeds and cultivated plants. Phytoplasmas are prokaryotic plant pathogens that colonize the sieve elements of their host plant, causing severe alterations in phloem function and impairment of assimilate translocation.
21p visilicon2711 20-08-2021 15 1 Download
-
Water deficiency is likely to become more frequent and intense as a result of global climate change, which may severely impact agricultural production in the world.
14p vijichea2711 28-05-2021 11 1 Download
-
In people with albinism (PWA), the deficiency of melanin increase the risk of skin cancers. The aim of this study was to determine the prevalence of skin cancers and characteristics of these detected skin cancers (histological types, localization) in PWA in 10 cities in Togo in 2019.
5p vianrose2711 27-04-2021 9 2 Download