cafe au lait macules neurofibromatosis | Cafe Au Lait Macules

Keyword	CPC	PCC	Volume	Score	Length of keyword
cafe au lait macules neurofibromatosis	0.94	0.4	6244	99	38
cafe	1.77	0.5	8405	72	4
au	0.24	0.7	3127	55	2
lait	0.35	0.3	3982	1	4
macules	1.85	0.8	7488	18	7
neurofibromatosis	1.26	0.9	2168	67	17

Keyword	CPC	PCC	Volume	Score
cafe au lait macules neurofibromatosis	0.71	0.5	6546	21
neurofibromatosis cafe au lait	0.7	0.6	5378	47
cafe au lait neurofibromatosis type 1	0.57	0.8	2477	86
cafe au lait spots and neurofibromatosis	0.63	0.3	9908	9
neurofibromatosis cafe au lait spots	0.53	0.5	4142	3
cafe au lait spots neurofibromatosis type 1	0.64	0.9	1112	3
neurofibromatosis type 2 cafe au lait spots	1.89	0.3	280	53
neurofibromatose cafe au lait flecken	0.45	1	906	2
neurofibroma cafe au lait spots	1.7	0.2	6916	53
cafe au lait macules	1.44	1	1197	27
cafe au lait macula	0.35	0.1	9554	52
cafe au lait disease	0.54	0.9	1055	79
cafe au lait syndrome	0.27	0.1	766	48
cafe au lait nf1	0.21	0.2	8112	78
cafe au lait dermatology	0.56	0.2	657	93
cafe ole spots neurofibromatosis	1.89	1	1581	72

Search Results related to cafe au lait macules neurofibromatosis on Search Engine

Cafe Au Lait Macules - StatPearls - NCBI Bookshelf
nih.gov

https://www.ncbi.nlm.nih.gov/books/NBK557492/

WEBJul 31, 2023 · Neurofibromatosis type 2 (NF2) NF2 is a different disorder from NF1, both clinically and genetically. It occurs due to a mutation in the NF2 gene located on chromosome 22, which produces merlin (tumor suppressor gene) and follows an autosomal dominant pattern of inheritance.

DA: 23 PA: 7 MOZ Rank: 58

Café-au-lait macule | DermNet
dermnetnz.org

https://dermnetnz.org/topics/cafe-au-lait-macule

WEBAug 30, 2017 · They may be isolated or associated with systemic diseases such as neurofibromatosis (NF), McCune Albright syndrome, Legius syndrome, and Noonan syndrome with multiple lentigines syndrome. The overall prevalence of café-au-lait macules varies with race: 0.3% of Caucasians. 0.4% of Chinese. 3% of Hispanics.

DA: 9 PA: 62 MOZ Rank: 66

Neurofibromatosis 1 - GeneReviews® - NCBI Bookshelf
nih.gov

https://www.ncbi.nlm.nih.gov/books/NBK1109/

WEBOct 2, 1998 · Neurofibromatosis 1 (NF1) is a multisystem disorder characterized by multiple café au lait macules, intertriginous freckling, multiple cutaneous neurofibromas, and learning disability or behavior problems. About half of people with NF1 have plexiform neurofibromas, but most are internal and not suspected clinically.

DA: 76 PA: 16 MOZ Rank: 7

Treatment With Selumetinib for Café-au-Lait Macules and …
jamanetwork.com

https://jamanetwork.com/journals/jamadermatology/fullarticle/2813823

WEBNeurofibromatosis type 1 (NF1) is a rare autosomal dominant multisystem disorder resulting from NF1 variants that lead to the inactivation or downregulation of neurofibromin and consequent RAS/RAF/MEK/ERK signaling pathway activation.

DA: 40 PA: 21 MOZ Rank: 41

Revised diagnostic criteria for neurofibromatosis type 1 and
nature.com

https://www.nature.com/articles/s41436-021-01170-5

WEBMay 19, 2021 · Neurofibromatosis type 1 (NF1; OMIM 613113), inherited in an autosomal dominant pattern, is characterized by multiple café-au-lait macules (CALMs), skinfold freckling (more correctly...

DA: 78 PA: 58 MOZ Rank: 19

Neurofibromatosis type 1 (NF1): Pathogenesis, clinical ... - UpToDate
uptodate.com

https://www.uptodate.com/contents/neurofibromatosis-type-1-nf1-pathogenesis-clinical-features-and-diagnosis

WEBJan 22, 2024 · The hallmarks of NF1 are multiple café-au-lait macules and neurofibromas. The condition is called "segmental NF1" when clinical features are limited to one area of the body due to somatic mosaicism of a pathogenic variant in the neurofibromin 1 ( NF1) gene. The pathogenesis, clinical features, and diagnosis of NF1 are reviewed here.

DA: 72 PA: 16 MOZ Rank: 22

Café-au-lait Macules and Neurofibromatosis Type 1: A Review …
nih.gov

https://pubmed.ncbi.nlm.nih.gov/27212418/

WEBBackground: The first sign of neurofibromatosis type 1 (NF1) in a child is often the presence of multiple café-au-lait macules. Although previous studies reported that almost individuals with multiple café-au-lait macules will eventually develop NF1 based on clinical criteria, recent studies and clinical observations suggest that a ...

DA: 86 PA: 75 MOZ Rank: 5

An approach to café au lait macules in primary care setting
nih.gov

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8496705/

WEBSep 7, 2021 · CALMs may present as a manifestation of different syndromes such as neurofibromatosis Type 1 (NF1), McCune Albright syndrome, Fanconi's anemia, and tuberous sclerosis complex (TSC). [ 3] . CALMs are usually present after birth or in early age and can increase in number over time in some disorders such in NF1. [ 3] .

DA: 30 PA: 26 MOZ Rank: 33

Phenotypic variability among café-au-lait macules in neurofibromatosis …
nih.gov

https://pubmed.ncbi.nlm.nih.gov/20605257/

WEBAbstract. Background: Café-au-lait macules (CALMs) in neurofibromatosis type 1 (NF1) are an early and accessible phenotype in NF1, but have not been extensively studied. Objective: We sought to more fully characterize the phenotype of CALMs in patients with NF1.

DA: 90 PA: 28 MOZ Rank: 18

Café-au-lait Macules and Neurofibromatosis Type 1: A Review …
sciencedirect.com

https://www.sciencedirect.com/science/article/pii/S0887899416300133

WEBJul 1, 2016 · According to those criteria, NF1 is diagnosed when a patient has at least two of the followings: (1) six or more café-au-lait macules greater than 0.5 cm in the prepubertal child or greater than 1.5 cm after puberty; (2) skin-fold freckling; two or more neurofibromas of any type or one plexiform neurofibroma; (3) two or more Lisch nodules; (4) o...

DA: 14 PA: 84 MOZ Rank: 38