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495 Possible Causes for Eczema, Phenylketonuria

  • Eczema

    Sometimes eczema is used for describing atopic dermatitis as well as atopic eczema.[symptoma.com] […] adjective Comments on eczema What made you want to look up eczema ?[merriam-webster.com] […] ex-, yeast First Known Use: circa 1753 ECZEMA Defined for Kids Medical Dictionary Seen and Heard What made you want to look up eczema ?[web.archive.org]

  • Phenylketonuria

    The extent of the deficiency depends on the enzyme activity, complete deficiency causes phenylketonuria, with residual enzyme activity causing mild phenylketonuria.[symptoma.com] Clinical features in the untreated patient include mental retardation, defects in executive functioning, seizures, and eczema.[bestpractice.bmj.com] Clinical features in the untreated patient include intellectual disability, defects in executive functioning, seizures, and eczema.[bestpractice.bmj.com]

  • Hyperphenylalaninemia

    There were four cases (40%) with 6-pyruvoyl-tetrahydropterin synthase deficiency, three with GTP cyclohydrolase I - autosomal recessive form deficiency, and three with dihydropteridine[ncbi.nlm.nih.gov] PKU-like symptoms include eczema and fair hair and skin coloring. Causes Genetic defects in phenylalanine hydroxylase cause most cases of hyperphenylalaninemia.[emedicine.medscape.com] Due to a positive family history prenatal diagnosis for phenylketonuria was performed, revealing heterozygosity for classic phenylketonuria.[ncbi.nlm.nih.gov]

  • Classical Phenylketonuria

    ), PHENYLKETONURIA, PKU, PKU - Phenylketonuria, phenylalaninemia, phenylketonuria (diagnosis), phenylketonuria, Phenylalaninemia, Phenylketouria, Phenylketonuria - pku, Phenylketonurias[fpnotebook.com] Classical phenylketonuria is caused by a severe deficiency of phenylalanine hydroxylase and presents in infancy with developmental delay; seizures; skin hypopigmentation; eczema[icd9data.com] […] mood disorders, irregular motor functioning, and behavioral problems such as attention deficit hyperactivity disorder, as well as physical symptoms such as a "musty" odor, eczema[checkorphan.org]

  • Atopic Dermatitis

    […] herpetiformis Pemphigus foliaceus Graft-versus-host disease Dermatomyositis Metabolic disorders Zinc deficiency Pyridoxine ( vitamin B6) and niacin Multiple carboxylase deficiency Phenylketonuria[omicsonline.org] Breastfeeding mothers of babies with eczema need not change their own diet. Can eczema be cured? There is currently no cure for eczema.[healthywa.wa.gov.au] Triggers of eczema Some things make eczema more likely to appear.[betterhealth.vic.gov.au]

  • Food Allergy

    Adverse reactions to cow's milk associated with other conditions such as phenylketonuria and lactose intolerance may also be alleviated by the use of alternative formulas,[web.archive.org] Those with more severe hand eczema were more likely to suffer from allergic symptoms for foods, and diagnosed food allergy.[ncbi.nlm.nih.gov] Whilst the association between eczema and food allergy is well established, the role of dietary manipulation in children with eczema remains controversial.[ncbi.nlm.nih.gov]

  • Psoriasis

    […] psoriasis vulgaris, pemphigus, urticaria, pruritus, allergic contact dermatitis, fish odor syndrome, toxic oil syndrome, fixed drug eruption, genetic and metabolic disorders (phenylketonuria[doi.org] Eczema Eczema (also known as atopic dermatitis) can develop at any age, even during infancy. It usually begins before age 5.[verywell.com] This is one of the many natural eczema treatments you can customize to suit your specific needs.[rd.com]

  • Food Intolerance

    Metabolic food reactions are due to inborn or acquired errors of metabolism of nutrients, such as in lactase deficiency, phenylketonuria and favism.[en.wikipedia.org] There was no significant difference in infant eczema (eight studies, 2558 infants, typical RR 0.84, 95% CI 0.68, 1.04), childhood eczema incidence (two studies, 950 infants[ncbi.nlm.nih.gov] Parents frequently associate FI with eczema, hives, chronic diarrhoea and hyperactivity.[ncbi.nlm.nih.gov]

  • Homocystinuria

    In phenylketonuria, the L-arginine/NO pathway seems not be altered.[ncbi.nlm.nih.gov] Cutaneous signs of homocystinuria include: Hypopigmentation due to inhibition of tyrosinase Fair and thin hair Thin, translucent skin Hyperhidrosis Dry skin with tendency to eczema[dermnetnz.org] […] oxidase SUOX (12q13)* Biochemical profile: Elevated urine sulfite, thiosulfate, and S-sulfocysteine; decreased sulfate Clinical features: Developmental delay, ectopia lentis, eczema[merckmanuals.com]

  • Phenylalanine Increased

    Editorial (1979) The growing problems of phenylketonuria. Lancet II: 1381–1383 Google Scholar 14.[link.springer.com] Symptoms can include microcephaly, epilepsy, mental retardation, behavior problems, eczema, pigmentation lighter than the family constellation, decreased myelin formation,[invitae.com] Untreated individuals have very fair hair, eczema, a mousy odor of the urine and skin, and progressive mental retardation.[medical-dictionary.thefreedictionary.com]

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