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19 Possible Causes for Glucose Decreased, Round Face in Infancy

  • Glycogen Storage Disease Type 1

    Infants have a round “doll” face.[clinicaladvisor.com] […] of maternal glucose), and the decrease continues.[emedicine.medscape.com] […] in water fluid) Treatment [ edit ] Glucose drinks during the day Infusion at night through a nasogastric tube Cornstarch throughout the day for older children Dietary restrictions[en.wikibooks.org]

  • Glycogen Storage Disease Type 3

    Infants have a round “doll” face.[clinicaladvisor.com] […] tolerance. 5 The patient was a 20 year old woman who had acanthosis nigricans and decreased glucose tolerance.[jmg.bmj.com] G-1-P to glucose ratio as compared with normal controls).[nature.com]

  • Glycogen Storage Disease due to Muscle Phosphorylase Kinase Deficiency

    Infants have a round “doll” face.[clinicaladvisor.com] The patients have severe hypoglycemia, hyperlipidemia (increased lipolysis caused by decreased glucose), uricemia (caused by competitive inhibition by lactate of renal tubular[edusanjalbiochemist.blogspot.com] […] a) Decreased uptake of glucose by peripheral cells b) Abnormal response to glucagon c) Decreased glucagon to insulin ratio d) Decreased glucose output by the liver e) Increased[namrata.co]

  • Pseudopseudohypoparathyroidism

    A 62 year old man with a height of 171.5 cm, a round face, a short neck, central obesity and brachydactyly had normal ranges of serum calcium, phosphorus and PTH and a normal[e-enm.org] Pseudohypoparathyroidism with decreased glucose tolerance; report of a case. J Clin Endocrinol Metab. 1950; 10 (12):1609–15. [ PubMed ] [ Google Scholar ] 25.[ncbi.nlm.nih.gov] […] proteolysis decreases glucose capitation (CONTRAREGULATOR) -- hyperglucemiant function of somatotropic cells in adipose tissue decrease capitation of glucose increase lipolysis[brainscape.com]

  • Glycogen Storage Disease Type 6

    Infants have a round “doll” face.[clinicaladvisor.com] […] in water fluid) Treatment [ edit ] Glucose drinks during the day Infusion at night through a nasogastric tube Cornstarch throughout the day for older children Dietary restrictions[en.wikibooks.org] […] illness with decreased oral intake.[emedicine.com]

  • Glycogen Storage Disease due to GLUT2 Deficiency

    Infants have a round “doll” face.[clinicaladvisor.com] Prolonged hyperglycaemia after glucose loading indicates decreased utilization of glucose. The cause of this metabolic defect is unknown.[slideheaven.com] Renal tubular dysfunction is characterized by a specific pattern of impaired proximal tubular transport mechanisms, with marked impairment of glucose transport.[scinapse.io]

  • Glycogen Storage Disease Type 9

    Infants have a round “doll” face.[clinicaladvisor.com] The resulting glucose enters the blood stream When blood glucose level is high (immediately after meal) 1. Glucagon levels decrease 2.[quizlet.com] In fact, consuming carbohydrates exacerbates exercise intolerance because glucose decreases the blood concentration of alternative fuels such as free fatty acids and ketones[doi.org]

  • Barth Syndrome

    In early childhood, the face is round with full cheeks and an overall “cherubic” appearance (see Figure 8 ), whereas after the first decade and especially after puberty, the[ncbi.nlm.nih.gov] Kiebish adds that boys with Barth syndrome do not metabolize amino acids, fatty acids and glucose correctly because mutations in the tafazzin (TAZ) gene decrease the remodeling[outlook.wustl.edu] Younger males with Barth syndrome have a characteristic facial gestalt that is most evident during infancy, characterized by a tall and broad forehead, round face, full cheeks[ncbi.nlm.nih.gov]

  • Char Syndrome

    Note the round face with full cheeks, hypertelorism, epicanthal folds, and apparently low-set ears. Child with cri-du-chat syndrome.[emedicine.medscape.com] Some trials have decreased the methotrexate dosage, increasing the dose only if tolerated.[atlasgeneticsoncology.org] Cri-du-chat syndrome is an autosomal deletion syndrome caused by a partial deletion of chromosome 5p and is characterized by a distinctive, high-pitched, catlike cry in infancy[emedicine.medscape.com]

  • Mosaic Monosomy X

    Microcephaly Round, moonlike face Wide-set, downward-slanting eyes Strabismus Epicanthal folds Williams syndrome Type of abnormality: deletion Critical region: 7q11.23 Mental[alpfmedical.info] Markers serum alpha-fetoprotein (AFP): decreased beta HCG elevated if hydrops present decreased if no hydrops serum inhibin elevated if hydrops present absent if hydrops absent[radiopaedia.org] […] simple, low-set ears with preauricular pits or tags Cri-du-chat syndrome Type of abnormality: deletion Critical region: 5p15.2 Mental deficiency High-pitched catlike cry in infancy[alpfmedical.info]

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