Results 1 to 10 of about 3,562 (228)

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   +4 more sources

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

Biologics: Targets & 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 ...
Binkhonain FK, Aldokhayel S, BinJadeed H, Madani A   +3 more
doaj   +4 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   +3 more sources

Spontaneous subconjunctival abscess in congenital lamellar ichthyosis

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   +5 more sources

Photoletter to the editor: Lamellar ichthyosis and arthrogryposis in a premature neonate. [PDF]

J Dermatol Case Rep, 2015
Lamellar ichthyosis is a rare congenital disorder characterized by collodion membrane at birth and facial anomalies (eclabium and ectropion). The major underlying genetic defect is in TGM1, with mutations of this gene found in 50% of patients. An early diagnosis is fundamental in view of establishing a specific treatment due to the severity of the ...
De Leonibus C, Lembo C, Santantonio A, Fioretti T, Rojo S, Salvatore F, De Vivo M, Esposito G, Giliberti P.   +8 more
europepmc   +7 more sources

Congenital bilateral ectropion in lamellar ichthyosis

Oman Journal of Ophthalmology, 2011
Chandana Chakraborti, Partha Tripathi, Gautam Bandopadhyay, Dayal Bandhu Mazumder   +3 more
doaj   +5 more sources

A case of lamellar ichthyosis with rickets and carcinoma of the hypopharynx

Indian Journal of Dermatology, 2014
Lamellar ichthyosis (LI) is an autosomal recessive disorder rarely associated with systemic organ involvement and development of carcinoma. Rickets has occasionally been described with LI owing to impaired vitamin D synthesis following altered ...
Aditya Kumar Bubna, Mahalakshmi Veeraraghavan, Sankarasubramaniam Anandan, Sudha Rangarajan   +3 more
doaj   +5 more sources

Vitamin D Status in Distinct Types of Ichthyosis: Importance of Genetic Type and Severity of Scaling [PDF]

Acta Dermato-Venereologica, 2021
Data on vitamin D status of patients with inherited ichthyosis in Europe is scarce and unspecific concerning the genetic subtype. This study determined serum levels of 25-hydroxyvitamin D3 (25(OH)D3) in 87 patients with ichthyosis; 69 patients were ...
Mi-Ran Kim, Vinzenz Oji, Frederic Valentin, Heiko Traupe, Jerzy-Roch Nofer, Ingrid Hausser, Hans Christian Hennies, Katja Eckl, Stefan A. Wudy, Alberto Sánchez-Guijo, Laura Kerschke, Judith Fischer, Kira Süßmuth   +12 more
doaj   +3 more sources

Lamellar ichthyosis with rickets. [PDF]

Pak J Med Sci, 2013
Lamellar ichthyosis (LI) is a rare genetic disorder with autosomal recessive inheritance. It is equally seen in both sexes and usually manifests at birth. The child presents as a collodion baby. The erythema is minimal or absent; but when present, it is maximum on the face. The scaling is generalized, accentuated on lower extremities and flexural areas.
Ali R, Aman S, Nadeem M.
europepmc   +4 more sources

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

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