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624 Possible Causes for Eczema, Headache, Phenylketonuria

  • Food Allergy

    Her vomiting, which was preceded by objective torque vertigo, headache and weakness, had been recurring with constant frequency every two months since she was 3 years old.[] 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,[] Whilst the association between eczema and food allergy is well established, the role of dietary manipulation in children with eczema remains controversial.[]

  • Toxoplasmosis

    Some people, however, develop signs and symptoms similar to those of the flu, including: Body aches Swollen lymph nodes Headache Fever Fatigue In people with weakened immune[] […] amniocentesis procedures) and overall costs. 11, 12 However, proponents of universal screening argue that screening occurs for even less common diseases, such as neonatal phenylketonuria[] Neonatal screenings also exist in the United States for several inborn errors of metabolism, even though the numbers of affected infants are very small (annual incidence of phenylketonuria[]

  • Classical Phenylketonuria

    […] incidence of eczema among those off the diet (28% vs. 11% on-diet); hyperactivity (14% vs. none on-diet); lethargy and lack of energy (19% vs. none on- diet); recurrent headaches[] ), PHENYLKETONURIA, PKU, PKU - Phenylketonuria, phenylalaninemia, phenylketonuria (diagnosis), phenylketonuria, Phenylalaninemia, Phenylketouria, Phenylketonuria - pku, Phenylketonurias[] Classical phenylketonuria is caused by a severe deficiency of phenylalanine hydroxylase and presents in infancy with developmental delay; seizures; skin hypopigmentation; eczema[]

  • Food Intolerance

    The most common symptoms were bowel symptoms, tiredness, stomach symptoms, and headaches.[] Metabolic food reactions are due to inborn or acquired errors of metabolism of nutrients, such as in lactase deficiency, phenylketonuria and favism.[] 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[]

  • Celiac Disease

    We present a 39-year-old woman with celiac disease who was on gluten-free diet for 8 years and presented with diarrhea, headache, insomnia, loss of appetite, abnormal taste[] […] oligopeptidase autoimmune disease Exogenous enzymes are being tested or already used orally to treat several diseases, including pancreatic insufficiency, lactose intolerance, and phenylketonuria[] Assessment for publication bias in analyses of eczema was not possible because of the limited number of studies.[]

  • Fabry Disease

    Cerebrovascular/Central Nervous System Problems Dizziness or vertigo, headache, and early stroke are all cerebrovascular symptoms of Fabry disease.[] Phenylketonuria (PKU) 1 was the first disorder screened in newborns.[] Severe pain in the feet, high fevers, headaches, constipation and fatigue. These were all symptoms our son Blake started experiencing at the age of 5 1/2.[]

  • Phenylketonuria

    And many people have reported the following side effects from aspartame: Fibromyalgia Syndrome and symptoms of Fibromyalgia Multiple Sclerosis symptoms Dizziness Headaches[] 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.[]

  • Pityriasis Circinata

    […] rashes: Are often pink or pale red Are oval in shape May be scaly May follow lines in the skin or appear in a "Christmas tree" pattern May itch Other symptoms may include: Headache[] Dermatol Surg. 34:1-4. 2008 Associated conditions It is seen in: albinism idiopathic guttate hypomelanosis leprosy leucism Phenylketonuria pityriasis alba vitiligo Angelman[] Alice Related Q&As Ringworm Dry skin and Eczema help Cure for psoriasis? Allergic to exercise?[]

  • Hyperphenylalaninemia

    The most common adverse reactions (incidence 4%) were headache, rhinorrhea, pharyngolaryngeal pain, diarrhea, vomiting, cough, and nasal congestion.[] 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.[]

  • Woodhouse Sakati Syndrome

    pyruvoyl-tetrahydropterin synthase deficiency Charcot-Marie-Tooth disease type 2B Odontoma dysphagia syndrome Glycogen storage disease type 0, liver Vagneur Triolle Ripert[] […] results in a 2-year period, or 0.53%, compared with 6.36% for biotinidase deficiency, 1.84% for congenital hypo-thyroidism, 0.56% for classic galactosemia, and 2.9% for phenylketonuria[] […] partial lipodystrophy associated with PPARG mutations Saul Wilkes Stevenson syndrome Cartilage-hair hypoplasia Nguyen syndrome Glanzmann thrombasthenia Jacobsen syndrome 6-[]

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