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ichthyosis

Synonyms

Noun

1. genetic disease

2. genetic disorder, genetic abnormality, genetic defect, congenital disease, inherited disease, inherited disorder, hereditary disease, hereditary condition

Usage
Immunomodulatory Therapy May Reduce Some Comorbidities in Congenital Ichthyosis - Dermatology Advisor
Noninvasive Tape Strips Detect Immune and Epidermal Hyperplasia Markers in Major Orphan Ichthyoses - Medscape
Azitra's ATR-01 Shows Promise in Preclinical Studies for Ichthyosis Vulgaris - Dermatology Times
A case report of X-linked ichthyosis associated with epilepsy due to an Xp22.31 deletion fragment - Frontiers
Effective Management of Mosaic Epidermolytic Ichthyosis in a Pediatric Patient With Urea 30% Cream: A Case Report - Wiley Online Library
Harlequin ichthyosis: a comprehensive review of pathogenesis, diagnosis, and management - EurekAlert!
Meet Maddie: The Inspirational 18-Year-old Living with Rare Skin Condition Ichthyosis - checkupnewsroom.com
College Student with Rare Skin Condition Hopes to 'Shed the Stigma' - TODAY.com
Azitra, Inc. Announces Positive Preclinical Data for ATR-01 Program, Designed to Treat Ichthyosis Vulgaris - PR Newswire
Harlequin Ichthyosis in a Preterm Neonate: A Case Report - Cureus
Azitra reports positive preclinical data for ichthyosis treatment - Investing.com
Informing guidelines for managing X-linked ichthyosis: expert commentary - Hospital Healthcare Europe
Phase 3 Setback for TMB-001 Spurs Hopeful Out-Licensing of Vehicle in Congenital Ichthyosis - Dermatology Times
Newborn Born With Rare Harlequin Ichthyosis Genetic Disorder In Borkhola - Barak Bulletin
Woman Born with a '1‑in‑a‑Million' Skin Condition Says She Just Wants to Live a 'Normal Life' (Exclusive) - People.com
Parents of Hong Kong’s ‘Girl Behind the Face’ finally share their story - South China Morning Post
Neonatal Epidermolytic Ichthyosis Caused by a KRT10 Mutation (c.467G>A, p.Arg156His): A Case Report - Wiley Online Library
Ichthyosis Severity Score Shows Reliability in Skin of Color - Medscape
Expanded Phenotypic Spectrum of Cerebral Dysgenesis, Neuropathy, Ichthyosis, and Keratoderma (CEDNIK) Syndrome: A Rare Case Featuring Supraventricular Tachycardia and Tethered Spinal Cord - Cureus
Genetic Study Yields Personalized Therapeutics for a Rare Skin Disorder - Dermatology Times
Harlequin ichthyosis: The rare genetic disease that gives babies hard 'scales' - Live Science
Defying the Odds: A Case of Successfully Treated Harlequin Ichthyosis in Lebanon - Wiley Online Library
New guidelines for identifying increased risk of psychological and heart conditions in rare skin condition - Cardiff University
Successful Treatment of Two Rare Pediatric Keratinization Disorders wi | PTT - Dove Medical Press
Deep molecular response on asciminib combined with imatinib in patient with chronic myeloid leukemia and ichthyosis resistant and intolerant to monotherapy with other TKIs | Ząber | Acta Haematologica Polonica - Via Medica Journals
Ichthyosis vulgaris: An updated review - Jaffar - 2023 - Skin Health and Disease - Wiley Online Library
Inside the little-known disease that causes babies to be born with hard scales - New York Post
Old drugs shed new light on a rare skin disease - Drug Discovery News
Dupilumab improves congenital ichthyosis - Wiley Online Library
X‐linked ichthyosis: New insights into a multi‐system disorder - Wren - 2022 - Skin Health and Disease - Wiley Online Library
Scientists develop first gene-editing treatment for skin conditions - Medical Xpress
Yale tests a treatment for skin diseases that often target children - YaleNews
The Rare Genetic Condition Where Your Skin Doesn’t Play By The Rules: Epidermolytic Ichthyosis Explained - ETV Bharat
Skin Deeper: How Skin Diseases Affect the Patient Beyond the Surface - Future of Personal Health -
Treatment of Lamellar Ichthyosis in a 10‐Year‐Old Child With Secukinumab - Wiley Online Library
A novel combination of mutations leading to congenital ichthyosis and ichthyosis vulgaris - Wiley Online Library
Dental Abnormalities in Congenital Ichthyoses: Case Report and Review of the Literature - Wiley Online Library
Ichthyosis Prematurity Syndrome - Li - 2025 - Australasian Journal of Dermatology - Wiley Online Library
She Has Ichthyosis Confetti, A Rare Genetic Skin Disorder, And She's Opening Up About What It's Like - Chip Chick
Presentation of ichthyosis after substrate reduction therapy in Gaucher type 1 - Wiley Online Library
Ichthyosis as a manifestation of fetal gaucher - Anales de Pediatría
X-linked ichthyosis presenting with cryptorchidism for orchidopexy: A rare anesthetic encounter and case report - Wiley Online Library
Ichthyosis - Nature
Ichthyosis Market Expected to Grow at a CAGR of 4.28% during 2025-2035, Impelled by Advancements in Novel Therapies - BioSpace
Harlequin Ichthyosis Nanobubble Hydrotherapy: A Breakthrough in Treatment - Cureus
Autosomal recessive congenital ichthyosis: CERS3 mutations identified by a next generation sequencing panel targeting ichthyosis genes - Nature
Mom shares son’s struggle with rare condition causing skin to look like scales - TODAY.com
Identification of novel FATP4 mutations in a Japanese patient with ichthyosis prematurity syndrome - Nature
Managing Ichthyosis in the General Dermatology Office - Dermatology Times
Harlequin Ichthyosis: Symptoms, survival rate, and treatment options explained - India TV News
'Never been so humiliated': Woman asked to leave flight because of skin condition - TODAY.com
Assessing the Use of Ustekinumab in a Pediatric Patient With Harlequin Ichthyosis - Cureus
Connexin hemichannel inhibition ameliorates epidermal pathology in a mouse model of keratitis ichthyosis deafness syndrome - Nature
Recent Advances in the Genetics and Management of Harlequin Ichthyosis - Ahmed - 2014 - Pediatric Dermatology - Wiley Online Library
Topical Isotretinoin Shows Promise in Phase 3 ASCEND Trial for Congenital Ichthyosis - Dermatology Times
Increased melanocytic nevi and lentigines in two patients with harlequin ichthyosis - Wiley Online Library
TMB-001 for Congenital Ichthyosis Subtypes Tested by Dermatologists - Dermatology Times
Baby with rare skin condition abandoned at Italian hospital - BBC
Christopher Bunick, MD, PhD: Efficacy, Safety of TMB-001 in Treating Congenital Ichthyosis - HCPLive
Staying positive despite having a challenging condition - The Straits Times
‘When a mother flees from her newborn’ – comparing Harlequin Ichthyosis cases in Nigeria and the United Kingdom. - blogs.biomedcentral.com
Biogeographical origin and timing of the founder ichthyosis TGM1 c.1187G > A mutation in an isolated Ecuadorian population - Nature
Acquired ichthyosis associated with IgG4-related disease - The Lancet
Clinical and genetic findings in 13 Chinese children with keratinopathic ichthyosis - Yang - 2023 - Pediatric Investigation - Wiley Online Library
Two cases of KRT1 mutation-associated epidermolytic ichthyosis without typical epidermolytic hyperkeratosis in the neonatal skin lesions - Wiley Online Library
Eye Surgeon Helps a Young Boy Blink Again - UC San Diego Today
Positive Results from Phase 2b Study of TMB-001 for Congenital Ichthyosis - Dermatology Times
Epidermolytic Ichthyosis in a Neonate: A Case Study - medtalks.in
Novel transglutaminase 1 mutations in patients affected by lamellar ichthyosis - Nature
Ichthyosis, psoriasiform dermatitis, and recurrent fungal infections in patients with biallelic mutations in PERP - Wiley Online Library
Topical isotretinoin ointment shows ‘reassuring’ efficacy, safety in congenital ichthyosis - Healio
Transplanting Epidermal Autografts to Treat Epidermolytic Ichthyosis - EMJ
Foundation for Ichthyosis & Related Skin Types Now Accepting Letters of Intent for 2025 Research Grant Program - Dermatology Times
Inherited ichthyoses/generalized Mendelian disorders of cornification - Nature
What is harlequin-type ichthyosis, the strange ‘fish skin’ disease? - EL PAÍS English
Harlequin ichthyosis: A case report of severe presentation in Eritrea - Wiley Online Library
Ocular features in ichthyosis follicularis, alopecia, and photophobia syndrome - Eye - Nature
Novel Scoring System Shows Promise in Assessing Severity of Ichthyosis - AJMC
CLDN1 Arg81His founder variant causes ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis (ILVASC) syndrome in Moroccan Jews - Wiley Online Library
Harlequin ichthyosis: A case image from Syria - Al‐Dabbagh - 2022 - Clinical Case Reports - Wiley Online Library
Alan Mendelsohn, MD, Shares Insights Into Congenital Ichthyosis Patient Care and the Development of TMB-001 - Dermatology Times
Loss-of-function mutations in the gene encoding filaggrin cause ichthyosis vulgaris - Nature
Filaggrin mutations p.R501X and c.2282del4 in ichthyosis vulgaris - Nature
Veterinary Dermatology | ACVD & ESVD Journal - Wiley Online Library
Shwachman‐Diamond Syndrome Presenting as Neonatal Ichthyosis - Jacinto‐Calimag - 2025 - Pediatric Dermatology - Wiley Online Library
Yale team finds new genetic cause of ichthyosis, identifies Accutane as potential treatment - Fierce Biotech
3D model of harlequin ichthyosis reveals inflammatory therapeutic targets - JCI.org
This Rare Skin Condition Used To Be A Death Sentence. Now Sufferers Are Living Full Lives. - All That's Interesting
Epidermolytic Ichthyosis in a Neonate - The Journal of Pediatrics
TMB-001 yields encouraging results in congenital ichthyosis subtypes - Healio
Scabies in a 14‐year‐old girl with superficial epidermolytic ichthyosis - Vázquez‐Osorio - 2022 - Pediatric Dermatology - Wiley Online Library
Ichthyosis Scoring System Reliable in Measuring Global Ichthyosis Severity - HCPLive
Study Finds Novel Pathogenic Variants, Inflammatory Cytokines, and Activated JAK-STAT Signaling in Patients With Congenital Ichthyosis - Dermatology Times
Ichthyosis in sarcoidosis: a rare skin manifestation of a systemic disease - The Lancet
Putting It All Together: Postmortem Diagnosis of a Rare Ichthyosis Syndrome - Cureus
Disseminated tinea incognita in a patient with ichthyosis vulgaris and eczema - Wiley Online Library
A baby girl who 'never stops smiling' is living with a rare condition that makes her skin crack - Business Insider
Progress in addressing a severe skin disease that affects dogs and humans - Penn Today
A mutation in the SREBF1 gene resulting in autosomal-dominant ichthyosis Follicularis, Atrichia, and photophobia syndrome - Wiley Online Library
Amy Paller, MD: Long-Term Outlook for EB, Ichthyosis and Netherton Syndrome Treatment - HCPLive
Foreign Language Equivalents
Foreign Language Equivalents of 'ichthyosis'
Language Equivalent   Language Equivalent
French    Spanish
Misspellings - Typos
ichthyosia,   ichtthyosis,   ichthyyosis,   ichthyossi,   ichyhyosis,   ichthyoiss,   ichthoysis,   ichthypsis,   ichtyhosis,   icchthyosis,   ichrhyosis,   ichthyoss,   uchthyosis,   chthyosis,   ixhthyosis,   iichthyosis,   ichthyois,   ichthysois,   ichthyosus,   icthhyosis,   ichthyosiss,   ihthyosis,   ichthtosis,   ichthosis,   ihcthyosis,   ichtyosis,   icthyosis,   icjthyosis,   ichtjyosis,   cihthyosis,   ichhtyosis,   ichthhyosis,   ichhyosis,   ochthyosis,   ichthuosis,   ichthyodis,   ichtgyosis,   ichthyoosis,   icgthyosis,   ivhthyosis,   ichthyoais,   ichthyosi,   ichthyisis,   ichthyosid,   ichthyosos,   ichthyossis,   ichthyosiis,   ichthysis,   ichhthyosis
Words Starting with Letter - 'A'
a a battery a billion
a bit a bit much a capella singing
a cappella singing a couple of a few
a fortiori a good deal a great deal
a horizon a hundred a hundred and one
a hundred thousand a hundred times a kempis
a la carte a la mode a level
a little a lot a million
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