GeneralConnection.com ➔ Dictionary
Dictionary Search

ichthyosis

Synonyms

Noun

1. genetic disease

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

Usage
Born with a Rare Skin Condition, 8-Year-Old Girl's Mood Changes in 'One Single Moment' During Wig Appointment (Exclusive) - People.com
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
A Case of Lamellar Ichthyosis in a Neonate from a Resource-Limited Set | IMCRJ - Dove Medical Press
Harlequin ichthyosis: a comprehensive review of pathogenesis, diagnosis, and management - EurekAlert!
Effective Management of Mosaic Epidermolytic Ichthyosis in a Pediatric Patient With Urea 30% Cream: A Case Report - Wiley Online Library
Azitra, Inc. Announces Poster Presentation at ASGCT 2026 Highlighting ATR-01 Program for Ichthyosis Vulgaris - PR Newswire
College Student with Rare Skin Condition Hopes to 'Shed the Stigma' - TODAY.com
Noninvasive Tape Strips Detect Immune and Epidermal Hyperplasia Markers in Major Orphan Ichthyoses - Medscape
Meet Maddie: The Inspirational 18-Year-old Living with Rare Skin Condition Ichthyosis - checkupnewsroom.com
Harlequin Ichthyosis in a Preterm Neonate: A Case Report - Cureus
Phase 3 Setback for TMB-001 Spurs Hopeful Out-Licensing of Vehicle in Congenital Ichthyosis - Dermatology Times
BREAKING THE CHAIN - SYNLAB
Veterinary Dermatology | ACVD & ESVD Journal - Wiley Online Library
Case Report: A family with X-linked ichthyosis identified by secondary findings of non-invasive prenatal testing - Frontiers
Azitra, Inc. Announces Positive Preclinical Data for ATR-01 Program, Designed to Treat Ichthyosis Vulgaris - PR Newswire
Successful Treatment of Two Rare Pediatric Keratinization Disorders wi | PTT - Dove Medical Press
Ichthyosis Severity Score Shows Reliability in Skin of Color - Medscape
Neonatal Epidermolytic Ichthyosis Caused by a KRT10 Mutation (c.467G>A, p.Arg156His): A Case Report - Wiley Online Library
Novel Topical CRISPR-based Therapy May Help Treat EB, Eczema, and Psoriasis - The Dermatology Digest
Teen Spends 45 Minutes Lotioning Her Body Every Morning Due to Rare ‘Achy, Itchy’ Skin Disorder (Exclusive) - People.com
Genetic Study Yields Personalized Therapeutics for a Rare Skin Disorder - Dermatology Times
Woman Born with a '1‑in‑a‑Million' Skin Condition Says She Just Wants to Live a 'Normal Life' (Exclusive) - People.com
Harlequin ichthyosis: The rare genetic disease that gives babies hard 'scales' - Live Science
Azitra's skin bacteria therapy cut water loss in pig skin tests - Stock Titan
The pathophysiology of genetic ichthyoses includes the composition of the cellular surface region of cornified cells - EurekAlert!
Harlequin ichthyosis awareness: ‘My girl is a fighter!’ - thatslife.com.au
Old drugs shed new light on a rare skin disease - Drug Discovery News
Adult-Onset Acquired Ichthyosis Revealing an Underlying Colon Adenocarcinoma - Cureus
First successful treatment of epidermolytic Ichthyosis with Vunakizumab: A Case Report - Frontiers
Defying the Odds: A Case of Successfully Treated Harlequin Ichthyosis in Lebanon - Wiley Online Library
Yale tests a treatment for skin diseases that often target children - YaleNews
Netherton Syndrome: A Systematic Review of the Challenges of Diagnosis and Treatment - Cureus
X‐linked ichthyosis: New insights into a multi‐system disorder - Wren - 2022 - Skin Health and Disease - Wiley Online Library
Newborn Born With Rare Harlequin Ichthyosis Genetic Disorder In Borkhola - Barak Bulletin
Ichthyosis vulgaris: An updated review - Jaffar - 2023 - Skin Health and Disease - Wiley Online Library
The Rare Genetic Condition Where Your Skin Doesn’t Play By The Rules: Epidermolytic Ichthyosis Explained - ETV Bharat
Dupilumab improves congenital ichthyosis - Wiley Online Library
Clinical Diagnosis and Management Challenges of Harlequin Ichthyosis in a Preterm Neonate: A Case Report From Uganda - Wiley Online Library
Neonatal Erythroderma: Diagnostic Challenges and the Limitations of Genetic Testing - Cureus
A Case of Ichthyosis Vulgaris and the Use of 70% Glycolic Acid Chemical Peels for Management - Cureus
Topical Isotretinoin Shows Promise in Phase 3 ASCEND Trial for Congenital Ichthyosis - Dermatology Times
Ichthyosis Prematurity Syndrome - Li - 2025 - Australasian Journal of Dermatology - Wiley Online Library
Presentation of ichthyosis after substrate reduction therapy in Gaucher type 1 - Wiley Online Library
Dental Abnormalities in Congenital Ichthyoses: Case Report and Review of the Literature - Wiley Online Library
Harlequin Ichthyosis Nanobubble Hydrotherapy: A Breakthrough in Treatment - Cureus
A novel combination of mutations leading to congenital ichthyosis and ichthyosis vulgaris - Wiley Online Library
Managing Ichthyosis in the General Dermatology Office - Dermatology Times
Congenital Ichthyosis Update - The Dermatology Digest
Treatment of Lamellar Ichthyosis in a 10‐Year‐Old Child With Secukinumab - Wiley Online Library
TMB-001 for Congenital Ichthyosis Subtypes Tested by Dermatologists - Dermatology Times
Ichthyosis - Nature
Biogeographical origin and timing of the founder ichthyosis TGM1 c.1187G > A mutation in an isolated Ecuadorian population - Nature
Identification of novel FATP4 mutations in a Japanese patient with ichthyosis prematurity syndrome - Nature
Bullied but not beaten: Mui Thomas uses rare skin condition to inspire - CNN
Veterinary Dermatology | ACVD & ESVD Journal - Wiley Online Library
X-linked ichthyosis presenting with cryptorchidism for orchidopexy: A rare anesthetic encounter and case report - Wiley Online Library
Foundation for Ichthyosis & Related Skin Types Now Accepting Letters of Intent for 2025 Research Grant Program - Dermatology Times
Autosomal recessive congenital ichthyosis: CERS3 mutations identified by a next generation sequencing panel targeting ichthyosis genes - Nature
Positive Results from Phase 2b Study of TMB-001 for Congenital Ichthyosis - Dermatology Times
Novel Scoring System Shows Promise in Assessing Severity of Ichthyosis - AJMC
Ichthyosis Market Expected to Grow at a CAGR of 4.28% during 2025-2035, Impelled by Advancements in Novel Therapies - BioSpace
Connexin hemichannel inhibition ameliorates epidermal pathology in a mouse model of keratitis ichthyosis deafness syndrome - Nature
Staying positive despite having a challenging condition - The Straits Times
Harlequin ichthyosis: A case report and literature review - Wiley Online Library
‘When a mother flees from her newborn’ – comparing Harlequin Ichthyosis cases in Nigeria and the United Kingdom. - BMC blog network
Skin Barrier Dysfunction in Chronic Dermatoses: From Pathophysiology to Emerging Therapeutic Strategies - Cureus
Novel transglutaminase 1 mutations in patients affected by lamellar ichthyosis - Nature
Unknown mutations and genotype/phenotype correlations of autosomal recessive congenital ichthyosis in patients from Saudi Arabia and Pakistan - Wiley Online Library
Ichthyosis Skin Changes in a Patient With Hereditary Hemochromatosis - Cureus
Clinical and genetic findings in 13 Chinese children with keratinopathic ichthyosis - Yang - 2023 - Pediatric Investigation - Wiley Online Library
Ichthyosis in sarcoidosis: a rare skin manifestation of a systemic disease - The Lancet
Veterinary Dermatology | ACVD & ESVD Journal - Wiley Online Library
Mom shares son’s struggle with rare condition causing skin to look like scales - TODAY.com
Ophthalmic Review on Neonatal Harlequin Ichthyosis - Cureus
Study Finds Novel Pathogenic Variants, Inflammatory Cytokines, and Activated JAK-STAT Signaling in Patients With Congenital Ichthyosis - Dermatology Times
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
Recent Advances in the Genetics and Management of Harlequin Ichthyosis - Ahmed - 2014 - Pediatric Dermatology - Wiley Online Library
Harlequin ichthyosis: A case report of severe presentation in Eritrea - Wiley Online Library
Yale team finds new genetic cause of ichthyosis, identifies Accutane as potential treatment - Fierce Biotech
Alan Mendelsohn, MD, Shares Insights Into Congenital Ichthyosis Patient Care and the Development of TMB-001 - Dermatology Times
'Never been so humiliated': Woman asked to leave flight because of skin condition - TODAY.com
Epidermolytic Ichthyosis in a Neonate - The Journal of Pediatrics
Progress in addressing a severe skin disease that affects dogs and humans - Penn Today
Ocular features in ichthyosis follicularis, alopecia, and photophobia syndrome - Eye - Nature
Loss-of-function mutations in the gene encoding filaggrin cause ichthyosis vulgaris - Nature
Two cases of KRT1 mutation-associated epidermolytic ichthyosis without typical epidermolytic hyperkeratosis in the neonatal skin lesions - Wiley Online Library
A baby girl who 'never stops smiling' is living with a rare condition that makes her skin crack - Business Insider
What is harlequin-type ichthyosis, the strange ‘fish skin’ disease? - EL PAÍS English
The rare genetic disease that gives babies hard 'scales' - Yahoo
Epidermolytic Ichthyosis in a Neonate: A Case Study - medtalks.in
Mid-South woman born with rare skin condition dies unexpectedly - Action News 5
Harlequin ichthyosis: A case image from Syria - Al‐Dabbagh - 2022 - Clinical Case Reports - Wiley Online Library
Topical isotretinoin ointment shows ‘reassuring’ efficacy, safety in congenital ichthyosis - Healio
Topical Use of Isotretinoin Shows Promise as Treatment For Congenital Ichthyosis - Dermatology Times
New guidelines for identifying increased risk of psychological and heart conditions in rare skin condition - Cardiff University
Oral vitamin D versus acitretin in congenital non-syndromic ichthyosis: double blinded, randomized controlled trial - Wiley Online Library
CLDN1 Arg81His founder variant causes ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis (ILVASC) syndrome in Moroccan Jews - Wiley Online Library
Skin permeability barrier formation by the ichthyosis-causative gene FATP4 through formation of the barrier lipid ω-O-acylceramide - PNAS
Filaggrin mutations p.R501X and c.2282del4 in ichthyosis vulgaris - Nature
Foreign Language Equivalents
Foreign Language Equivalents of 'ichthyosis'
Language Equivalent   Language Equivalent
French    Spanish
Misspellings - Typos
,   ichhyosis,   ichtthyosis,   ichthysis,   ichthtosis,   ichthyodis,   ichthyisis,   icgthyosis,   ichthypsis,   ichthyoiss,   icchthyosis,   ichhthyosis,   iichthyosis,   ichrhyosis,   ochthyosis,   chthyosis,   ichthosis,   ichthyoais,   uchthyosis,   ichthyoss,   ichthyyosis,   ichthhyosis,   ichthyosia,   ichthyosi,   ichthyosiis,   cihthyosis,   ivhthyosis,   ixhthyosis,   ichthyosus,   ichtyhosis,   ichthyois,   ichthysois,   ichthyossi,   ichthyoosis,   ichtyosis,   ichthuosis,   ichthyossis,   ichtjyosis,   icthhyosis,   ichtgyosis,   ichhtyosis,   ihthyosis,   ichthyosiss,   ichthyosid,   icjthyosis,   ichthyosos,   icthyosis,   ichthoysis,   ihcthyosis,   ichyhyosis
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
Go to Page 1              Go to Page 2 »   
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z