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744 Possible Causes for Eczema, Phenylketonuria

  • Histidinemia

    Of 34.5 million babies tested for phenylketonuria, 3000 cases have been diagnosed in time to prevent mental retardation by means of dietary therapy.[books.google.ro] The urinary histamine levels of patients with eczema-like dermatitis were twice that of those without dermatitis.[ncbi.nlm.nih.gov] Abstract As a result of mass testing for phenylketonuria in infants and retarded children with the urinary ferric chloride test, a new entity, histidinemia, was described[annals.org]

  • Eczema

    Sometimes eczema is used for describing atopic dermatitis as well as atopic eczema.[symptoma.com] To examine differences in demographic factors, lifestyle factors and severity between subgroups of hand eczema patients, with a focus on hyperkeratotic hand eczema.[ncbi.nlm.nih.gov] Asteatotic eczema (eczema craquelé, xerotic eczema) occurs most frequently in areas of dehydrated skin, most often during the winter months when decreased humidity results[ncbi.nlm.nih.gov]

  • 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 intellectual disability, defects in executive functioning, seizures, and eczema.[bestpractice.bmj.com] Clinical features in the untreated patient include mental retardation, defects in executive functioning, seizures, and eczema.[bestpractice.bmj.com]

  • Brandt Syndrome

    […] enteropathica-like skin lesions in the perioral and diaper area, not responding to oral zinc or antimicrobials, conditions like biotin deficiency, essential fatty acid deficiency, phenylketonuria[ijdvl.com] In addition, they have a clear demarcation and may resemble eczema or psoriasis.[symptoma.com] The lesions may resemble eczema or develop further into coated cysts (crusted vesicles), pustules or bullas.[herbs2000.com]

  • 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]

  • 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

    An extract from a liver biopsy of a patient with classical phenylketonuria contains phenylalanine 4-hydroxylase (EC 1.14.3.1) with a specific activity 0.27% of the normal[ncbi.nlm.nih.gov] 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]

  • Penicillin G

    —Some strengths of the amoxicillin chewable tablets contain aspartame, which is changed by the body to phenylalanine, a substance that is harmful to patients with phenylketonuria[goodrx.com] In individuals predisposed to develop allergic disease(s), the sequence of sensitization and clinical manifestations proceed as follows: eczema and respiratory disease (rhinitis[mayomedicallaboratories.com] History of or suspected allergy (asthma, eczema, hay fever, hives); history of allergy to cephalosporins; kidney or liver dysfunction, myasthenia gravis, epilepsy, neonates[robholland.com]

  • 6-Pyruvoyl-Tetrahydropterin Synthase Deficiency

    Long-term follow-up and adult outcome of 6-pyruvoyl-tetrahydropterin synthase deficiency.[biomedsearch.com] Chorea , athetosis , hypersalivation , rash with eczema , and sudden death have also been reported.[en.wikipedia.org] Printed in the Netherlands Korean IEM Workshop 1993 Prenatal Diagnosis of 6-Pyruvoyl Tetrahydropterin Synthase Deficiency in Seven Subjects H. SHINTAKU 1, K. J.[myslide.es]

  • Ranitidine

    It can be dangerous to use Generic Ranitidina if you suffer from or have a history of kidney disease, liver disease,phenylketonuria (PKU), porphyria.[generalhlthnews.org] He presented rash in the face and eczema on the dorsum of the hands with itching. The study by prick tests with ranitidine gave negative response.[ncbi.nlm.nih.gov] Hyper-immunoglobulin E (IgE) syndrome (HIES) is a rare primary immunodeficiency characterized by eczema, recurrent skin and lung infections, elevated serum IgE, and multiple[clinicaltrials.gov]

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