Meeting abstracts
BAD 2026
British Association of Dermatologists · Manchester, 30 June – 2 July 2026
639 abstracts, published in BJD on 26 June 2026.
- BH16
Early-onset onychodysplasia with multisystem ectodermal features in a toddler: a diagnostic challenge
Ahmed H, Constantinou S, … senior author Takwale A
- BI07
Skin as the clue: cutaneous manifestations of VEXAS syndrome in a tertiary centre cohort
Blyth R, Trikha R, … senior author Basu T
- BI42
Chronic lower-leg ulceration in a patient with X-linked hypogammaglobulinaemia: Helicobacter bilis identified as culprit organism via metagenomics pathogen detection
Earnshaw C, Baptista Gonçalves R, … senior author Farquharson N
- CPC14
Keratoacanthoma in Muir–Torre syndrome: diagnostic confidence enables conservative management
Sexton F, Carr R, … senior author Murphy LA
- DP02
Improving Lynch syndrome screening in sebaceous neoplasms: integrating the Mayo Muir–Torre score to overcome limitations of mismatch repair immunohistochemistry
Lashin S, Kareem A, … senior author Elsheikh S
- DP15
A case series of four patients with elastosis perforans serpiginosa with differing predisposing factors
Doyle C, Timoney I, … senior author O’Connor C
- DP17
Categorizing BAP1-inactivated melanocytic tumours using dermoscopic and clinical features with correlation to pathology
Craig S, Wright D, … senior author Smith H
- DP22
VEXAS syndrome presenting with histiocytoid Sweet syndrome-like skin changes
Sehrawat M, McPherson K, Ghaffar S
- GD02
Understanding risk factors to strengthen skin cancer surveillance programmes for people with albinism in East Africa
Roberts E, Mataiga R, … senior author Freeland H
- HX08
From ‘children who burn in sunlight’ to DNA repair defect: xeroderma pigmentosum and the birth of molecular dermatology
McGarel S, Da Silva F, … senior author Fleming S
- P017
- P074
Mainstreaming genetic testing in dermatology: an audit of diagnostic yield and frequency of variants of uncertain significance
Robinson P, Carson L, … senior author Rajan N
- P076
A multicentre evaluation of surveillance outcomes and phenotypic trends in carriers of CDKN2A pathogenic variants
Nicholls I, Robinson P, … senior author Willsmore Z
- P142
Making the invisible visible: national epidemiology reporting of rare dermatological diseases in England
Zhao H, Hardy S, … senior author Venables ZC
- P171
National prevalence and mortality risk of epidermolysis bullosa in the UK: insights from primary care and linked hospital data
Chien HY, Savva G, … senior author Richardson K
- P173
Topical statins for porokeratosis: targeting the mevalonate pathway – a systematic review and evidence map
Shanshal M, Uthayakumar A, … senior author Bala L
- PA03
- PA10
- PA11
- PA14
Piecing together Carney complex
Taibjee S, Poudel P, … senior author Lovgren ML
- PD04
Clinical spectrum and outcomes in a cohort of patients with trichothiodystrophy: a single-centre experience
White J, Sellar P, … senior author Paolino A
- PD05
Xeroderma pigmentosum complementation group C: a retrospective observational study of 46 patients reveals skin cancer heterogeneity dependent on the level of nucleotide excision DNA repair
Theocharopoulos I, Balgos K, … senior author Fassihi H
- PS31
- PSD03
Isolated genital angiokeratomas: an under-recognized cutaneous marker of Fabry disease revealed by dermoscopy
Baraz S, Baba R, … senior author Hjira N
- SG01
- SG02
Screening and genetic testing pathways for sebaceous tumours to identify Muir–Torre syndrome
Zaki F, Matin RN, Ieremia E
- SG07
- SG08
Pathogenic variants in the PSENEN and NCSTN genes cause ‘follicular’ Dowling–Degos disease: report of five unrelated Indian families
Gupta V, Khandpur S, … senior author Krishna Yenamandra V
- SG09
Vulvovaginal involvement and sexual dysfunction in women with ichthyosis: a cross-sectional questionnaire study
Theocharopoulos I, Doolan B, … senior author Mellerio J
- SG10
Features of paediatric pachyonychia congenita (KRT6A/6B/6C/16/17-pEDD)
McCarthy R, O’Toole E
- SG11
- SG12
Unmasking of Muir–Torre syndrome following tacrolimus-based immunosuppression
Belgi S, Schirwani S
- SG13
A case series of four patients with elastosis perforans serpiginosa with differing aetiologies
Doyle C, Timoney I, … senior author O’Connor C
- SG14
JAK of all trades: successful use of upadacitinib in treatment of epidermolysis bullosa pruriginosa
Yiu D, Bardhan A, … senior author Heagerty A
- SG15
Superimposed mosaicism in tuberous sclerosis complex presenting as unilateral facial angiofibromas
Hoban J, Leahy M, … senior author Sadlier M
- SG16
A case of laryngo-onycho-cutaneous syndrome: a rare form of junctional epidermolysis bullosa
Dawood S, Chadha M, Hatfield S
- SG17
Familial progressive hyper- and hypopigmentation due to a novel variant in KITLG
Grantham H, Cullup T, … senior author Wilson B
- SG18
When telomeres are too long: multiple melanoma in situ revealing a germline POT1 mutation
Safta Y, Granahan A, … senior author Collier N
- SG19
Warts and all? A 14-year update on the world’s first renal transplantation in a patient with junctional epidermolysis bullosa
Yiu D, Harper N, … senior author Heagerty A
- SG20
Acral peeling skin syndrome mimicking epidermolysis bullosa simplex
Victory L, Baird J, … senior author Murrell D
- SG21
Recalcitrant Darier disease with severe pain, chronic infection and multisystem complications: therapeutic challenges and the role of radiotherapy
Sexton F, O’ Connell M, … senior author Irvine AD
- SG22
The cardiocutaneous conundrum and the role of multidisciplinary management
Godwin A, Ying Pua Q, Devine D
That's every abstract.