Spitz Nevus
What's New
Last Posted: Apr 03, 2020
- Utility of p16-Ki-67-HMB45 score in sorting benign from malignant Spitz tumors.
Garola Robert et al. Pathology, research and practice 2019 Oct 215(10) 152550 - CLINGEN Actionability Report for Tumor Predisposition Syndrome - BAP1
ClinGen Actionability Working Group - Identification of HRAS mutations and absence of GNAQ or GNA11 mutations in deep penetrating nevi.
Bender Ryan P, et al. Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc 2013 10 (10) 1320-8 - Spitz nevus
From NCATS Genetic and Rare Diseases Information Center
Content Summary
Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Eclampsia
- Erythema Multiforme
- Familial Mediterranean Fever
- Fragile X Syndrome
- Gaucher Disease
- Glomerulonephritis
- Graves Disease
- Hemophilia
- Huntington Disease
- Microcephaly
- Myasthenia Gravis
- Phenylketonuria
- Retinitis Pigmentosa
- Severe Combined Immunodeficiency
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- Page last reviewed:Feb 1, 2024
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