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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.[] The urinary histamine levels of patients with eczema-like dermatitis were twice that of those without dermatitis.[] 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[]

  • Eczema

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

  • Phenylketonuria

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

  • 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[] In addition, they have a clear demarcation and may resemble eczema or psoriasis.[] The lesions may resemble eczema or develop further into coated cysts (crusted vesicles), pustules or bullas.[]

  • Homocystinuria

    In phenylketonuria, the L-arginine/NO pathway seems not be altered.[] 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[] […] oxidase SUOX (12q13)* Biochemical profile: Elevated urine sulfite, thiosulfate, and S-sulfocysteine; decreased sulfate Clinical features: Developmental delay, ectopia lentis, eczema[]

  • 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[] PKU-like symptoms include eczema and fair hair and skin coloring. Causes Genetic defects in phenylalanine hydroxylase cause most cases of hyperphenylalaninemia.[] Due to a positive family history prenatal diagnosis for phenylketonuria was performed, revealing heterozygosity for classic phenylketonuria.[]

  • Classical Phenylketonuria

    An extract from a liver biopsy of a patient with classical phenylketonuria contains phenylalanine 4-hydroxylase (EC with a specific activity 0.27% of the normal[] Classical phenylketonuria is caused by a severe deficiency of phenylalanine hydroxylase and presents in infancy with developmental delay; seizures; skin hypopigmentation; eczema[] […] 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[]

  • 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[] In individuals predisposed to develop allergic disease(s), the sequence of sensitization and clinical manifestations proceed as follows: eczema and respiratory disease (rhinitis[] History of or suspected allergy (asthma, eczema, hay fever, hives); history of allergy to cephalosporins; kidney or liver dysfunction, myasthenia gravis, epilepsy, neonates[]

  • 6-Pyruvoyl-Tetrahydropterin Synthase Deficiency

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

  • 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.[] 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.[] Hyper-immunoglobulin E (IgE) syndrome (HIES) is a rare primary immunodeficiency characterized by eczema, recurrent skin and lung infections, elevated serum IgE, and multiple[]

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