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Literature DB >> 1750770

Family implications of neonatal Gorlin's syndrome.

Abstract

Two very preterm infants (born at 29 and 25 weeks, respectively) were found to have abnormal ribs. Though this was thought unimportant at the time, it was subsequently shown to indicate that some members of their families had a dominantly inherited risk of developing skin cancer and other serious problems.

Entities: Disease Species

Mesh：

Year: 1991 PMID： 1750770 PMCID： PMC1590282 DOI： 10.1136/adc.66.10_spec_no.1162

Source DB: PubMed Journal: Arch Dis Child ISSN： 0003-9888 Impact factor: 3.791

1 in total

Review 1. Nevoid basal-cell carcinoma syndrome.

Authors: R J Gorlin
Journal: Medicine (Baltimore) Date: 1987-03 Impact factor: 1.889

1 in total

7 in total

1. Intronic splicing mutations in PTCH1 cause Gorlin syndrome.

Authors: Zaynab Bholah; Miriam J Smith; Helen J Byers; Emma K Miles; D Gareth Evans; William G Newman
Journal: Fam Cancer Date: 2014-09 Impact factor: 2.375

2. A Case of Gorlin-Goltz Syndrome Presented With Multiple Odontogenic Keratocysts in the Jaw Without Skin Manifestation.

Authors: A Rupesh Rao; Amar Taksande
Journal: Cureus Date: 2022-05-02

3. Nevoid Basal Cell Carcinoma Syndrome: A Long-Term Study in a Family.

Authors: Thiago de Santana Santos; André Vajgel; Paulo Ricardo Saquete Martins-Filho; Almir Walter de Albuquerque Maranhao Filho; Ricardo José De Holanda Vasconcellos; Riedel Frota; José Rodrigues Laureano Filho
Journal: Craniomaxillofac Trauma Reconstr Date: 2015-08-03

Family implications of neonatal Gorlin's syndrome.

Review 1. Nevoid basal-cell carcinoma syndrome.

1. Intronic splicing mutations in PTCH1 cause Gorlin syndrome.

2. A Case of Gorlin-Goltz Syndrome Presented With Multiple Odontogenic Keratocysts in the Jaw Without Skin Manifestation.

3. Nevoid Basal Cell Carcinoma Syndrome: A Long-Term Study in a Family.

4. Gorlin-Goltz syndrome.

5. Gorlin-goltz syndrome.

6. Gorlin-Goltz syndrome: A rare case report.

7. Gorlin-Goltz Syndrome: Case report and literature review.