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972 Possible Causes for Disturbance of Growth, Failure to Thrive

  • Cystinosis

    Growth retardation improved after correction of electrolyte disturbances, the initiation of cysteamine therapy and treatment with recombinant human growth hormone.[ncbi.nlm.nih.gov] The history of muscle weakness, failure to thrive, polydipsia, and polyuria prompted subsequent clinical and laboratory evaluations, leading to the correct diagnosis of cystinosis[ncbi.nlm.nih.gov] Clinically the disorder shows a slowly progressive glomerular insufficiency rather than the prominent Fanconi syndrome, electrolyte and water disturbances, growth arrest,[ncbi.nlm.nih.gov]

  • Esophagitis

    In children there can be difficulties with nutrition and poor growth, vomiting/regurgitation (sick going up and down, which can disturb sleep), food refusal (fussy eating)[gutscharity.org.uk] It presents with failure to thrive, nausea, and vomiting in children and is a common reason for dysphagia and food impaction in adults.[ncbi.nlm.nih.gov] Dysphagia Chest or upper abdominal pain Food stuck in the esophagus Heartburn that doesn’t respond to medication Regurgitation In children: vomiting, poor weight gain or failure[nm.org]

  • Erythroderma Desquamativum

    Decreased zinc absorption resulting from diarrhea may further aggravate the condition, leading to a vicious cycle. 5 Other extracutaneous features include growth retardation[consultant360.com] Blogs Submit your blog on Generalized Erythroderma, Diarrhea, And Failure To Thrive to be featured![novusbio.com] […] to thrive .[malacards.org]

  • Progressive Familial Intrahepatic Cholestasis

    Both patients had normal gamma-glutamyl transpeptidase levels, but showed severe pruritus with sleep disturbance, cholestasis, jaundice and growth failure.[ncbi.nlm.nih.gov] This usually leads to failure to thrive, cirrhosis, and the need for liver transplantation.[en.wikipedia.org] At follow-up, biochemical parameters improved significantly, growth was regained, relief in pruritus, sleeping pattern was normalized.[ncbi.nlm.nih.gov]

  • Hypertension

    ; diabetes mellitus Acral features; large hands and feet; frontal bossing Serum growth hormone 1 ng/mL during oral glucose load Elevated age- and sex-matched IGF-1 level;[dx.doi.org] Relevant information includes the following: Prematurity Bronchopulmonary dysplasia History of umbilical artery catheterization Failure to thrive History of head or abdominal[web.archive.org] […] hypokalemia) Low aldosterone and renin Urinary cortisol metabolites; genetic testing Acromegaly S5.4-16 Rare Acral features, enlarging shoe, glove, or hat size; headache, visual disturbances[doi.org]

  • Diencephalic Syndrome

    Seizure: rarely described as a presenting feature Focal motor weakness: rarely described as a presenting feature Intellectual disturbance or somnolence: most likely to be[emedicine.medscape.com] KEYWORDS: failure to thrive; infant health[ncbi.nlm.nih.gov] BACKGROUND: Diencephalic syndrome (DS) is a rare cause of failure to thrive in early childhood.[ncbi.nlm.nih.gov]

  • Vitamin B12 Deficiency

    The team looked at changes in soil phosphorus (an essential nutrient for tree growth) and how much disturbance there had been in the soils after harvesting.[sci.waikato.ac.nz] When preventive supplementation has failed, one should recognize and treat quickly an infant presenting with failure to thrive and delayed development.[ncbi.nlm.nih.gov] Vitamin B 12 deficiency causes anaemia, fatigue, mood disturbance and other neuropsychiatric and neurological complications.[doi.org]

  • Distal Renal Tubular Acidosis

    disturbance.[merckmanuals.com] We suggest that RTA be considered a diagnostic possibility in all children with failure to thrive and nephrocalcinosis.[ncbi.nlm.nih.gov] We report an unusual case of 5-yrs-old girl presenting with recurrent episodic weakness with documented hypokalemia, polyuria and failure to thrive.[ncbi.nlm.nih.gov]

  • Bartter's Disease

    disturbance Late childhood to adulthood Neuromuscular symptoms (eg, muscle spasms, weakness) Uncommon or mild Common Both syndromes are usually autosomal recessive, although[merckmanuals.com] Clinical findings Proximal muscle weakness, failure to thrive, short stature, convulsions, tetany, cramps, ileus, gout, mental retardation, enuresis, nocturia, polyuria, salt[medical-dictionary.thefreedictionary.com] […] hormone deficiency, disturbances in vasopressin secretion and empty sella: a new hereditary renal tubular-pituitary syndrome?.[jmedicalcasereports.biomedcentral.com]

  • CAMFAK Syndrome

    However, a very small ossification center may underline a disturbance of epiphyseal growth, related either to a local event (trauma,infection,osteochondrosis) or to a systemic[rrnursingschool.biz] Diseases related to Cataract, Microcephaly, Failure to Thrive, Kyphoscoliosis Syndrome via text searches within MalaCards or GeneCards Suite gene sharing: Human phenotypes[malacards.org] Research of Cataract, Microcephaly, Failure To Thrive, Kyphoscoliosis Syndrome has been linked to Microcephaly, Hereditary Diseases, Failure To Thrive, Peripheral Neuropathy[novusbio.com]

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