Results 1 to 10 of about 4,231 (126)

Successful Treatment of an Adult with Atopic Dermatitis and Lamellar Ichthyosis Using Dupilumab [PDF]

Biologics: Targets and Therapy, 2022
Faisal K Binkhonain, Sara Aldokhayel, Hessah BinJadeed, Abdulaziz Madani Dermatology Department, College of Medicine, King Saud University, Riyadh, Saudi ArabiaCorrespondence: Abdulaziz Madani, Dermatology Department, King Saud University, Riyadh, 7805 ...
Hessah Binjadeed, Faisal Binkhonain
exaly   +4 more sources

An infant with lamellar ichthyosis presenting with meningitis [PDF]

Clinical Case Reports, 2023
Lamellar ichthyosis is a rare congenital disorder characterized by widespread epidermal hyperkeratinization. It is a rare clinical disorder throughout the entire planet, and newborns with this disease frequently have collodion membranes (adhering, supple,
Telila Mesfin, Mesfin Tsegaye, Kenbon Seyoum, Girma Geta, Neway Ejigu, Tesfaye Elala, Degefa Gomora, Biniyam Sahiledengle, Eshetu Mesfin Tadesse, Getu Kusa, Teketel Tilahun   +10 more
doaj   +2 more sources

Spontaneous subconjunctival abscess in congenital lamellar ichthyosis [PDF]

Indian Journal of Ophthalmology, 2018
Congenital lamellar ichthyosis is an autosomal recessive, heterogeneous disorder presenting at birth with generalized skin involvement. The most common ophthalmic manifestation noted is bilateral ectropion of the lower eyelids.
Shivanand C Bubanale, Linda Maria Genoveva De Piedade Sequeira, Bhagyajyothi B Kurbet   +2 more
doaj   +2 more sources

Combined medical and surgical management for cicatricial ectropion in lamellar ichthyosis: A report of three cases [PDF]

Indian Journal of Ophthalmology, 2020
Ichthyosis is a rare inherited skin disorder characterized by abnormal keratinization of the epidermis. Cicatricial ectropion is the most common ophthalmic feature of congenital ichthyosis.
Nirmala Subramanian, Pratheeba Devi Nivean, Md Shahid Alam   +2 more
doaj   +2 more sources

Genu Valgum and Lamellar Ichthyosis: Insights into a Rare Presentation [PDF]

Journal of Orthopaedic Case Reports
Introduction: The main way that the skin produces Vitamin D, which is necessary for calcium metabolism and skeletal health, is through exposure to ultraviolet B rays.
Ajay Dodeja, Kirtee Meshram, Sushil Pande, Yash Shewale, Ruchika Nevse   +4 more
doaj   +2 more sources

Video Demonstration of ABCA12-Related Harlequin Ichthyosis in a Low-Resource Setting: Case Report and Review of Early Management Challenges. [PDF]

Clin Case Rep
ABSTRACT Harlequin ichthyosis is a rare, life‐threatening neonatal dermatologic emergency that can be confidently diagnosed clinically at birth. Prompt recognition and early supportive management—including thermoregulation, fluid balance, infection prevention, and intensive skin care—are crucial determinants of survival, especially in low‐resource ...
Elendu C, Amaechi DC, Elendu TC, Amaechi EC, Elendu ID, Okolo EH, Uyanwune MC.   +6 more
europepmc   +2 more sources

Multimodal Anterior Segment Imaging of Severe Mixed Exposure-Related Neurotrophic Keratopathy with Marked Corneal Thinning in Lamellar Ichthyosis [PDF]

Diagnostics
Lamellar ichthyosis is a rare congenital disorder of keratinization frequently associated with ocular complications, most commonly cicatricial ectropion and exposure keratopathy.
Wojciech Luboń, Małgorzata Luboń, Mariola Dorecka   +2 more
doaj   +2 more sources

Lamellar Ichthyosis in a Resource-Limited Setting: A Somaliland Case Report [PDF]

International Medical Case Reports Journal
Mohamed Osman Aw Hashi,1,2 Ahmed M Derie,3 Sadam Ismail Ahmed4 1College of medicine and surgery, University of Hargeisa, Hargeisa, Somaliland; 2Department of Dermatology and Venereology, Hargeisa Group Hospital, Hargeisa, Somaliland; 3Department of ...
Aw Hashi MO, Derie AM, Ahmed SI
doaj   +2 more sources

Pott disease in a 14-year-old girl affected by congenital lamellar ichthyosis type 3 and diabetes mellitus [PDF]

Journal of Global Infectious Diseases, 2018
Extrapulmonary manifestations of tuberculosis (TB) are particularly frequent during childhood, and usually involve the lymph nodes and the skull. They are related to predisposing immunosuppression conditions.
Maria Elena Cucuzza, Flavia La Mendola, Angela D'Ambra, Pierluigi Smilari, Filippo Greco, Agata Fiumara, Andrea D Praticò   +6 more
doaj   +2 more sources

Identification of Novel Mutation in the <i>ABCA12</i> Gene Causing Harlequin Ichthyosis. [PDF]

Clin Case Rep
ABSTRACT Harlequin ichthyosis (HI) is an uncommon and extremely severe hereditary condition that primarily affects the skin. Infants born with this disorder display dense skin and prominent diamond‐shaped plates that cover a significant portion of their bodies.
Soltani N, Bayati Z, Soosanabadi M, Zamani A, Lotfi A, Gholami M.   +5 more
europepmc   +2 more sources