Search Results - "EL FEKIH, Nadia"

Acrodermatitis enteropathica: a review of 29 Tunisian cases by KHARN, Monia, EL FEKIH, Nadia, AOUNALLAH-SKHIRI, Hajer, SCHMITT, Sébastien, FAZAA, Bécima, KÜRY, Sébastien, MOHAMED RIDHA KAMOUN

“…Acrodermatitis enteropathica is a rare autosomal recessive disease due to an abnormality in a zinc transporting molecule. We conducted a retrospective…”
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A delayed diagnosis of lepromatous leprosy: pitfalls and clues to early recognition by Kerkeni, Nadia, El Fékih, Nadia, Fazaa, Bécima, Zéglaoui, Faten, Mnif, Emna, Kamoun, Mohamed Ridha

“…Purpose  To remind special attention to atypical symptoms of Hansen’s disease, we report a case of an atypical case due to a delayed diagnosis. Background …”
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Transient symptomatic zinc deficiency in a breast-fed infant: Relevance of a genetic study by El Fékih, Nadia, M.D, Monia, Kharfi, M.D, Schmitt, Sebastien, M.D, Dorbani, Iméne, M.D, Küry, Sébastien, M.D, Kamoun, Mohamed R., M.D

“…Abstract Objective We present a case of acrodermatitis enteropathica in a full-term, breast-fed, 7-mo-old infant born from consanguineous parents with a family…”
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Lymphangiectasia of the vulva, treatment with CO 2 laser by Hamida, Myriam Ben, Baccouche, Dora, El Fekih, Nadia, Fazaa, Becima, Kamoun, Ridha

“…A pelvic magnetic resonance imaging (MRI) was performed and confirmed the presence of large myomas, without deep pelvic extension of lymphangioma. Because…”
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Oral HPV infection and MHC class II deficiency (A study of two cases with atypical outcome) by Guirat-Dhouib, Naouel, Baccar, Yemen, Mustapha, Imène Ben, Ouederni, Monia, Chouaibi, Sameh, El Fekih, Nadia, Barbouche, Mohamed Ridha, Fezaa, Bassima, Kouki, Ridha, Hmida, Slama, Mellouli, Fethi, Bejaoui, Mohamed

“…Major histocompatibility complex class II deficiency, also referred to as bare lymphocyte syndrome is a rare primary Immunodeficiency disorder characterized by…”
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Pigmented lesion in the inguinal region by El Fekih, Nadia, Hawiloo, Abdelmooti, Remmah, Soumeya, Zermani, Rachida, Fazaa, Becima

“…Pigmented Bowen disease (PBD) is a rare tumor characterized by increased melanin pigment in the epidermis or papillary dermis in addition to the typical…”
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Erythema elevatum diutinum: an "idiopathic" case by El Fekih, Nadia, Belgith, Ikram, Fazaa, Bécima, Remmah, Soumeya, Zéglaoui, Faten, Zermani, Rachida, Kamoun, Mohamed Ridha

“…Erythema elevatum diutinum (EED) is a rare condition with an unclear pathogenesis. Initially classified within neutrophilic dermatoses, it is now considered as…”
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Generalized peeling skin syndrome: Case report and review of the literature by Kharfi, Monia, Khaled, Aida, Ammar, Donia, Ezzine, Nadia, El Fekih, Nadia, Fazaa, Becima, Jaafoura, Hiabib, Kamoun, Mohamed Ridha

“…Peeling skin syndrome (PSS) is a rare form of ichthyosis with a probable autosomal recessive inheritance that exhibits superficial, painless, continual, or…”
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Childhood leishmaniasis: report of 106 cases by Kharfi, Monia, Benmously, Rym, El Fekih, Nadia, Daoud, Meriem, Fitouri, Zohra, Mokhtar, Inçaf, Ben Becher, Saïda, Kamoun, Mohamed Ridha

“…In Tunisia there are three epidemic clinical forms of cutaneous leishmaniasis. They are associated with three different species of Leishmania and are observed…”
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Pseudotumoral cutaneous aspergillosis in chronic granulomatous disease, report of a pediatric case by Khemiri, Monia, El fekih, Nadia, Borgi, Aida, Kharfi, Monia, Boubaker, Samir, Barsaoui, Sihem

“…Invasive aspergillosis is a life-threatening condition in patients with chronic granulomatous disease (CGD). Skin invasion by Aspergillus occurs most commonly…”
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A Missense Mutation in TGM5 Causes Acral Peeling Skin Syndrome in a Tunisian Family by Kharfi, Monia, El Fekih, Nadia, Ammar, Donia, Jaafoura, Habib, Schwonbeck, Susanne, van Steensel, Maurice A.M., Fazaa, Bécima, Kamoun, Mohamed Ridha, Fischer, Judith

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Histiocytosis X revealed by diabetes insipidus and skin lesions by El Fekih, Nadia, Kamoun, Inés, Jones, Meriem, Remmeh, Soummeya, Zéglaoui, Faten, Ben Slama, Claude, Fazaa, Bécima

“…Langerhans cell histiocytosis is part of a larger group of syndromes described as histiocytoses. The disease may involve single or multiple systems including…”
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Pigmentation cutanée isolée : penser à l'insuffisance surrénale by Badri, Talel, Zeglaoui, Faten, Khiari, Karima, El Fekih, Nadia, Fourati, Meriem, Fazaa, Becima, Kamoun, Mohamed Ridha

“…Addison's disease is a primary global deficiency in adrenocortical hormones resulting from the progressive total destruction of the adrenal glands. A…”
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Lymphangiectasia of the vulva, treatment with CO₂ laser by Hamida, Myriam Ben, Baccouche, Dora, El Fekih, Nadia, Fazaa, Becima, Kamoun, Ridha

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Kindler syndrome: clinical and ultra-structural particularities, a propos of three cases by El Fekih, Nadia, Mahfoudh, Anis, Zekri, Samy, Kharfi, Monia, Fazaa, Bécima, Jaafoura, Mohamed Habib, Kamoun, Mohamed Ridha

“…Kindler's syndrome is a rare type of genetic skin condition belonging to the class of bullous poikilodermia. We report three new sibling cases of this rare…”
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Bullosis diabeticorum: report of ten cases by El Fekih, Nadia, Zéglaoui, Faten, Sioud, Asma, Fazaa, Bécima, Kharfi, Monia, Gaigi, Sadok, Kamoun, Ridha

“…Bullosis diabeticorum is a rare characteristic complication of diabetes mellitus; it affects 0.5% of diabetics. Bullosis diabeticorum is a manifestation of…”
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Orf of the hand by Khaled, Aïda, Robbana, Feriel, Hammami, Houda, Kharfi, Monia, El Fekih, Nadia, Fazaa, Becima, Kamoun, Mohamed Ridha

“…The orf is a zoonotic infection which can be transmitted to humans. The aim of our report is to describe this often misdiagnosed viral infection in a man with…”
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Isolated cutaneous pigmentation: adrenal insufficiency may be the cause by Badri, Talel, Zeglaoui, Faten, Khiari, Karima, El Fekih, Nadia, Fourati, Meriem, Fazaa, Becima, Kamoun, Mohamed Ridha

“…Addison's disease is a primary global deficiency in adrenocortical hormones resulting from the progressive total destruction of the adrenal glands. A…”
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Hereditary ichthyosis in Tunisia: epidemiological study of 60 cases by Kharfi, Monia, El Fekih, Nadia, Ammar, Donia, Khaled, Aida, Fazaa, Bécima, Ridha Kamoun, Mohamed

“…Ichthyosis are a group of inherited keratinizing disorders. The cutaneous abnormalities may be isolated or associated with extra-cutaneous symptoms. To report…”
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What is new in the treatment of vitiligo by Khaled, Aida, Zeglaoui, Faten, Ezzine, Nadia, El Fekih, Nadia, Fazaa, Becima, Kamoun, Mohamed Ridha

“…Vitiligo is a frequent hypomelanosis that affects 1% of the world population, and 0,95% of the tunisian population. The objective of our study is to describe…”
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