CHECK THESE SAMPLES OF Congenital Localized Alopecia
Baldness or androgenic alopecia, on the other hand, is the incomplete or partial lack of hair (Bates, 2010).... Patchy loss of hair is a condition associated with alopecia areata (mild baldness) while total loss of air is associated with lopecia tatalis.... Conditions that lead to heart diseases include high cholesterol intake, diabetes, stroke, Artery Peripheral diseases, and congenital defects of the heart, metabolic syndrome, high blood pressure and use of cigarettes among others (Tjonnel, 1999)....
5 Pages
(1250 words)
Assignment
Pattern of inheritance congenital adrenal hyperplasia (CAH) refers to a group of autosomal recessive disorders that result enzyme denaturation and subsequently to deficiency in cortisol, aldosterone or both (Haldeman-Englert n.... ag.... Wilson n.... pag.... .... This means that a person with CAH can only be born from allele-carrying patients and/or clinically-presenting CAH individuals....
5 Pages
(1250 words)
Term Paper
congenital Erythropoietic Porphyria Porphyria is a group of diseases characterized by the deposition of porphyrins or porphyrin precursors due to a defect in one or more gene in the steps in the formation of enzymes such as Uroporphyrinogen III synthase (UROS) of the heme synthesis pathway.... CEP, or congenital erythropoietic porphyria is an autosomal recessive trait, which causes the patient to have an enlarged spleen and liver, reddish urine, bones and teeth as well as lesions on the skin that react to UV light due to the excess porphyrin deposits (Bishop et al....
5 Pages
(1250 words)
Research Paper
The paper "Color And congenital Blindness" discusses features of certain measures of blindness.... Blindness is a term that refers to the loss of visual perception due to psychological reasons or diseases and also due to physiological reasons and accidents.... hellip; The eye basically has two receptor cells in the retina, the cone cells, which are active in normal daylight and the rod cells which are active in low light conditions....
4 Pages
(1000 words)
Essay
congenital hypothyroidism (CHT) is a very common neonatal metabolic disorder, if untreated would results in severe neurodevelopmental impairment and infertility.... Usually, congenital hypothyroidism is sporadic, but 2% percent of thyroid dysgenesis is familial.... Genes associated with CHT are known to form two main groups:
Genes associated with the former include the TSH receptor in nonsyndromic congenital hypothyroidism, and Gsa and the thyroid transcription factors (TTF-1, TTF-2, and Pax-8)....
4 Pages
(1000 words)
Essay
In order to formally start this paper it is essential to state the crux of it all that is the definition of blindness, and more importantly color and congenital blindness.... This particular state is known as congenital blindness.... There is a growing threat of congenital blindness in the countries that are facing a food scarcity and have not been able to overcome it....
4 Pages
(1000 words)
Essay
Also known as congenital heart defect, cyanotic heart disease, heart defects or congenital cardiovascular malformations, it is the most common type of heart disease among… What causes this congenital condition is still unknown, but experts at the Texas Heart Institute have identified some factors that These are: congenital heart disease in the babys mother or father; congenital heart disease in the babys brother or sister; diabetes in the mother; German measles, toxoplasmosis (an infection that is passed through contact with cat feces), or HIV infection in the mother; the mothers use of alcohol during pregnancy; the mothers use of cocaine or other drugs during pregnancy; and the mothers use of certain over-the-counter and prescription medicines during pregnancy....
10 Pages
(2500 words)
Essay
The nondystrophic myotonia includes three main types: myotonia congenita, paramyotonia congenital, and hyperkalemic periodic paralysis.... However, Myotonia congenital (MC), a subtype of Myotonia, is a genetic muscle disease associated with defects in the musculoskeletal chlorine voltage-gated ion channels C1C-1....
8 Pages
(2000 words)
Term Paper