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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
Phase 3 Setback for TMB-001 Spurs Hopeful Out-Licensing of Vehicle in Congenital Ichthyosis - Dermatology Times
Azitra, Inc. Announces Poster Presentation at ASGCT 2026 Highlighting ATR-01 Program for Ichthyosis Vulgaris - PR Newswire
8-Year-Old Girl with Harlequin Ichthyosis Lights Up in Emotional Wig Appointment (Exclusive) - People.com
Harlequin Ichthyosis in a Preterm Neonate: A Case Report - Cureus
JEADV Clinical Practice | Clinical Dermatology and Venereology Journal - Wiley Online Library
FIRST Patient Voice Survey Finds Rare Skin Disease Takes Toll Far Beyond the Skin - Business Wire
Harlequin ichthyosis: a comprehensive review of pathogenesis, diagnosis, and management - EurekAlert!
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
Azitra's ATR-01 Shows Promise in Preclinical Studies for Ichthyosis Vulgaris - Dermatology Times
BREAKING THE CHAIN - SYNLAB
Veterinary Dermatology | ACVD & ESVD Journal - Wiley Online Library
Azitra, Inc. Announces Positive Preclinical Data for ATR-01 Program, Designed to Treat Ichthyosis Vulgaris - PR Newswire
Stylist Reveals Adaptations for Wig Appointment for 8-Year-Old with Rare Skin Condition (Exclusive) - People.com
Exploring Patterns of Palmar Hyperlinearity in Pediatric Population With Atopic Dermatitis or Ichthyosis Vulgaris Attending a Tertiary Care Hospital in Jaipur, India - Cureus
Teen Spends 45 Minutes Lotioning Her Body Every Morning Due to Rare ‘Achy, Itchy’ Skin Disorder (Exclusive) - People.com
Neonatal Epidermolytic Ichthyosis Caused by a KRT10 Mutation (c.467G>A, p.Arg156His): A Case Report - Wiley Online Library
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 awareness: ‘My girl is a fighter!’ - thatslife.com.au
Beyond the Skin: A Rare Disease Mandate Signals a Shift in Research - BriefGlance
The pathophysiology of genetic ichthyoses includes the composition of the cellular surface region of cornified cells - EurekAlert!
Old drugs shed new light on a rare skin disease - Drug Discovery News
‘The bomohs wanted to help’: Firdaus’s journey with ichthyosis - Free Malaysia Today
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
Ichthyosis Severity Score Shows Reliability in Skin of Color - Medscape
Dupilumab improves congenital ichthyosis - Wiley Online Library
Adult-Onset Acquired Ichthyosis Revealing an Underlying Colon Adenocarcinoma - Cureus
Netherton Syndrome: A Systematic Review of the Challenges of Diagnosis and Treatment - Cureus
Newborn Born With Rare Harlequin Ichthyosis Genetic Disorder In Borkhola - Barak Bulletin
Ocular Manifestations Leading to the Diagnosis of Ichthyosis: A Case Report - Cureus
Molecular Testing in Dermatology: Who and When to Test - Medscape
Topical Isotretinoin Shows Promise in Phase 3 ASCEND Trial for Congenital Ichthyosis - Dermatology Times
The Rare Genetic Condition Where Your Skin Doesn’t Play By The Rules: Epidermolytic Ichthyosis Explained - ETV Bharat
Multiple melanomas in ichthyosis with confetti: One more piece of evidence - Wiley Online Library
A Case of Ichthyosis Vulgaris and the Use of 70% Glycolic Acid Chemical Peels for Management - Cureus
Harlequin Ichthyosis Nanobubble Hydrotherapy: A Breakthrough in Treatment - Cureus
Ichthyosis Prematurity Syndrome - Li - 2025 - Australasian Journal of Dermatology - Wiley Online Library
Managing Ichthyosis in the General Dermatology Office - Dermatology Times
Veterinary Dermatology | ACVD & ESVD Journal - Wiley Online Library
TMB-001 for Congenital Ichthyosis Subtypes Tested by Dermatologists - Dermatology Times
Biogeographical origin and timing of the founder ichthyosis TGM1 c.1187G > A mutation in an isolated Ecuadorian population - Nature
Congenital Ichthyosis Update - The Dermatology Digest
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
Successful Treatment of an Adult with Atopic Dermatitis and Lamellar Ichthyosis Using Dupilumab - Dove Medical Press
Ichthyosis - Nature
Harlequin ichthyosis: A case report of severe presentation in Eritrea - Wiley Online Library
Treatment of Lamellar Ichthyosis in a 10‐Year‐Old Child With Secukinumab - Wiley Online Library
Positive Results from Phase 2b Study of TMB-001 for Congenital Ichthyosis - Dermatology Times
Presentation of ichthyosis after substrate reduction therapy in Gaucher type 1 - Wiley Online Library
Autosomal recessive congenital ichthyosis: CERS3 mutations identified by a next generation sequencing panel targeting ichthyosis genes - Nature
Connexin hemichannel inhibition ameliorates epidermal pathology in a mouse model of keratitis ichthyosis deafness syndrome - Nature
Assessing the Use of Ustekinumab in a Pediatric Patient With Harlequin Ichthyosis - Cureus
Harlequin ichthyosis: A case report and literature review - Wiley Online Library
A Unique Case of Harlequin Ichthyosis in the Tertiary Health Care System in a Rural Area - Cureus
Ichthyosis Market Expected to Grow at a CAGR of 4.28% during 2025-2035, Impelled by Advancements in Novel Therapies - BioSpace
X-linked ichthyosis presenting with cryptorchidism for orchidopexy: A rare anesthetic encounter and case report - Wiley Online Library
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
Expanded Phenotypic Spectrum of Cerebral Dysgenesis, Neuropathy, Ichthyosis, and Keratoderma (CEDNIK) Syndrome: A Rare Case Featuring Supraventricular Tachycardia and Tethered Spinal Cord - Cureus
Bullied but not beaten: Mui Thomas uses rare skin condition to inspire - CNN
Clinical and genetic findings in 13 Chinese children with keratinopathic ichthyosis - Yang - 2023 - Pediatric Investigation - Wiley Online Library
Amy Paller, MD: Long-Term Outlook for EB, Ichthyosis and Netherton Syndrome Treatment - HCPLive
An Overview of Harlequin Ichthyosis - Dermatology Times
Foundation for Ichthyosis & Related Skin Types Now Accepting Letters of Intent for 2025 Research Grant Program - Dermatology Times
Harlequin ichthyosis: The rare genetic disease that gives babies hard 'scales' - Live Science
Ichthyosis in sarcoidosis: a rare skin manifestation of a systemic disease - The Lancet
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. - BMC blog network
Mom shares son’s struggle with rare condition causing skin to look like scales - TODAY.com
Novel transglutaminase 1 mutations in patients affected by lamellar ichthyosis - Nature
Ocular features in ichthyosis follicularis, alopecia, and photophobia syndrome - Eye - Nature
Yale team finds new genetic cause of ichthyosis, identifies Accutane as potential treatment - Fierce Biotech
Unknown mutations and genotype/phenotype correlations of autosomal recessive congenital ichthyosis in patients from Saudi Arabia and Pakistan - Wiley Online Library
Recent Advances in the Genetics and Management of Harlequin Ichthyosis - Ahmed - 2014 - Pediatric Dermatology - Wiley Online Library
Ichthyosis Prematurity Syndrome: A Systematic Review of the Literature - Li - 2025 - Pediatric Dermatology - Wiley Online Library
Study Finds Novel Pathogenic Variants, Inflammatory Cytokines, and Activated JAK-STAT Signaling in Patients With Congenital Ichthyosis - Dermatology Times
Novel Scoring System Shows Promise in Assessing Severity of Ichthyosis - AJMC
Identification of novel FATP4 mutations in a Japanese patient with ichthyosis prematurity syndrome - Nature
Veterinary Dermatology | ACVD & ESVD Journal - Wiley Online Library
A baby girl who 'never stops smiling' is living with a rare condition that makes her skin crack - Business Insider
Ophthalmic Review on Neonatal Harlequin Ichthyosis - Cureus
Harlequin ichthyosis: A case image from Syria - Al‐Dabbagh - 2022 - Clinical Case Reports - Wiley Online Library
Two cases of KRT1 mutation-associated epidermolytic ichthyosis without typical epidermolytic hyperkeratosis in the neonatal skin lesions - Wiley Online Library
What is harlequin-type ichthyosis, the strange ‘fish skin’ disease? - EL PAÍS English
Epidermolytic Ichthyosis in a Neonate - The Journal of Pediatrics
Putting It All Together: Postmortem Diagnosis of a Rare Ichthyosis Syndrome - Cureus
Shwachman‐Diamond Syndrome Presenting as Neonatal Ichthyosis - Jacinto‐Calimag - 2025 - Pediatric Dermatology - Wiley Online Library
New guidelines for identifying increased risk of psychological and heart conditions in rare skin condition - Cardiff University
Mid-South woman born with rare skin condition dies unexpectedly - Action News 5
Pełny tekst: A Case of Self-Healing Collodion Baby, Monika Leończyk-Spórna - Przegląd Dermatologiczny 4/2025 - Termedia
Oral vitamin D versus acitretin in congenital non-syndromic ichthyosis: double blinded, randomized controlled trial - Wiley Online Library
Transplanting Epidermal Autografts to Treat Epidermolytic Ichthyosis - European Medical Journal
Loss-of-function mutations in the gene encoding filaggrin cause ichthyosis vulgaris - Nature
Ichthyosis Prematurity Syndrome: A Case Report and Review of Known Mutations - Kiely - 2014 - Pediatric Dermatology - Wiley Online Library
CLDN1 Arg81His founder variant causes ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis (ILVASC) syndrome in Moroccan Jews - Wiley Online Library
Foreign Language Equivalents
Foreign Language Equivalents of 'ichthyosis'
Language Equivalent   Language Equivalent
French    Spanish
Misspellings - Typos
ichtgyosis,   ichthyoosis,   ichthuosis,   chthyosis,   ichhyosis,   ixhthyosis,   ichthyosia,   ichthysois,   ichthosis,   ichthyosid,   ichthyossis,   ichthtosis,   ihthyosis,   ichthyoss,   uchthyosis,   icchthyosis,   ichthyodis,   ichthyosus,   ichthyosos,   ichthyyosis,   ichthyois,   icjthyosis,   ichthypsis,   ichthysis,   ichthyoiss,   ichthyossi,   ichthyoais,   ichtyhosis,   ivhthyosis,   ichtjyosis,   iichthyosis,   ichtthyosis,   ochthyosis,   ichthyosiis,   ichyhyosis,   ichtyosis,   ichrhyosis,   ichthhyosis,   ichthyisis,   ichhthyosis,   ichthoysis,   icthyosis,   ichhtyosis,   icthhyosis,   icgthyosis,   ichthyosi,   ihcthyosis,   ichthyosiss,   cihthyosis
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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