CYBERMED LIFE - ORGANIC  & NATURAL LIVING

Epidermolysis Bullosa

  • Improvement of renal function in epidermolysis bullosa patients after gluten free diet: two cases.

    Abstract Title:

    Improvement of renal function in epidermolysis bullosa patients after gluten free diet: two cases.

    Abstract Source:

    Eur Rev Med Pharmacol Sci. 2012 Oct ;16 Suppl 4:138-41. PMID: 23090831

    Abstract Author(s):

    G Annicchiarico, M G Morgese, L Brunetti, M Tampoia, L Garofalo, G Aceto, T Fiore, S Mauro, M Minelli

    Article Affiliation:

    Regional Coordination for Rare Diseases, Ares Puglia, Bari, Italy. This email address is being protected from spambots. You need JavaScript enabled to view it.

    Abstract:

    Epidermolysis bullosa (EB) is a rare inherited genetic disease characterized by an abnormal response of the skin and mucosa to mechanical trauma. Dystrophic EB (DEB) is very often associated with many extra cutaneous complications. Those complications involve either epithelial associated tissues or other organs. In particular, several renal complications have been described for DEB in the recessive form, such as amyloidosis, post-infection glomerulonephritis, upper and lower urinary tract obstruction and IgA-Nephropathy (IgAN). In the cases reported below we have two patients diagnosed with DEB that showed compromised renal function and proteinuria. The switch of the normal diet toward a gluten free diet resulted beneficial for both patients, since renal function was rescued and proteinuria cured. Moreover, a general health status improvement was recognised, given that nutritional condition was ameliorated and bone growing enhanced. Furthermore, in both patients the presence of autoantibodies anti-COL7 indicating an autoimmune form of the disease. Therefore, patients received low doses of betametasone useful to reduce inflammatory state and to control immune system function. In conclusion, our results prompt us to hypothesized that in these patients, due to the fragility of the intestinal mucosa, the absence in the diet of gluten may be beneficial.

  • Vitamin and trace metal levels in recessive dystrophic epidermolysis bullosa.

    Abstract Title:

    Vitamin and trace metal levels in recessive dystrophic epidermolysis bullosa.

    Abstract Source:

    J Eur Acad Dermatol Venereol. 2004 Nov;18(6):649-53. PMID: 15482288

    Abstract Author(s):

    S Ingen-Housz-Oro, C Blanchet-Bardon, M Vrillat, L Dubertret

    Abstract:

    BACKGROUND: In recessive dystrophic epidermolysis bullosa (RDEB), a good nutritional balance is necessary to obtain healing of the chronic wounds. However, involvement of the oral mucosa and oesophagus stenosis may be responsible for severe nutritional deficiencies. OBJECTIVE: In order to propose an adapted nutritional management, we studied the vitamin and trace metal status of 14 RDEB patients. METHODS: Height and weight were measured. Plasma levels of albumin, iron, ferritin, calcium, parathyroid hormone (PTH), folates, vitamins C, D, B12, A, E, B1, B6, PP and B2, zinc, selenium, carnitine and copper were measured. RESULTS: Most patients had a significant growth retardation. We found iron, vitamin D, C, B6, PP, zinc and selenium deficiencies in 36-70% of the patients, without clinical expression, except in one case. Vitamin B1, 12, B2, A/RBP, E/lipids and carnitine were normal. The three patients with gastrostomy feeding had better growth but still a protein deficiency and sometimes vitamin C, B6, PP, zinc and carnitine deficiencies. CONCLUSION: Vitamin and trace metal deficiencies are frequent in RDEB, even in patients receiving gastrostomy feeding, and often go unrecognized. Regular nutritional evaluation is necessary. Dietary advice and supplements should be given. Enteral feeding by gastrostomy should be discussed in early childhood.

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