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Article

A case of Brooke-Spiegler syndrome with a new mutation in the CYLD gene.

The British journal of dermatology - 1 May 2006

Heinritz W, Grunewald S, Strenge S, Schütz A, Froster U G, Glander H J, Paasch U, Simon J C

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Topics

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Share to Base Sequence
Share to Carcinoma, Adenoid Cystic
Share to Deubiquitinating Enzyme CYLD
Share to Head and Neck Neoplasms

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Skin Neoplasms

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Source

Identifiers

PMID: 16634909
DOI: 10.1111/j.1365-2133.2006.07142.x

Genes

CYLD

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 3 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A case of Brooke-Spiegler syndrome with a new mutation in the CYLD gene.PMID 16634909Read ↗

New mutation in the CYLD gene within a family with Brooke-Spiegler syndrome.Semantic proximity Read ↗

A case of Brooke-Spiegler syndrome with a novel germline deep intronic mutation in the CYLD gene leading to intronic exonization, diverse somatic mutations, and unusual histology.Semantic proximity Read ↗

Birt-Hogg-Dubé syndrome with novel FLCN gene mutations and different clinical presentations: Case series.Semantic proximity Read ↗

Birt-Hogg-Dubé syndrome in an African patient and a novel mutation in the FLCN gene.Semantic proximity Read ↗

A New Patient with NOCARH Syndrome Due to CDC42 Defect.Semantic proximity Read ↗

Phenotype–genotype correlations for clinical variants caused by CYLD mutationsSemantic proximity Read ↗

Developmental Phenotype of the Rare Case of DJ Caused by a Unique ADNP Gene De Novo MutationSemantic proximity Read ↗

Report of Three Novel Germline CYLD Mutations in Unrelated Patients with Brooke-Spiegler Syndrome, Including Classic Phenotype, Multiple Familial Trichoepitheliomas and Malignant Transformation.Semantic proximity Read ↗

Novel mutation in SPRED1: a sporadic case of Legius syndrome in an infant.Semantic proximity Read ↗

A novel large deletion of the CYLD gene causes CYLD cutaneous syndrome in a Chinese family.Semantic proximity Read ↗

A large family with CYLD cutaneous syndrome: medical genetics at the community levelSemantic proximity Read ↗

The cylindromatosis (CYLD) gene and head and neck tumorigenesisSemantic proximity Read ↗

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