Prevalence of Café-au-Lait Spots in children with solid tumors

Prevalence of Café-au-Lait Spots in children with solid tumors

Show other versions (1)

Abstract Cafe-au-lait maculae (CALM) are frequently observed in humans, and usually are present as a solitary spot. Multiple CALMs are present in a smaller fraction of the population and are usually associated with other congenital anomalies as part of many syndromes. Most of these syndromes carry a...

Bibliografske podrobnosti
Main Authors:	Anna Claudia Evangelista dos Santos, Benjamin Heck, Beatriz De Camargo, Fernando Regla Vargas
Format:	Article
Jezik:	English
Izdano:	Sociedade Brasileira de Genética 2016-01-01
Serija:	Genetics and Molecular Biology
Teme:	café-au-lait maculae pediatric solid tumors birth defects nosology
Online dostop:	http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572016005002104&lng=en&tlng=en

Podobne knjige/članki

Prevalence of Café-au-Lait Spots in children with solid tumors
od: Anna Claudia Evangelista dos Santos, et al.
Izdano: (2016-05-01)

Prevalence of Hypopigmented and Cafe-Au-Lait Spots in Idiopathic Epilepsy
od: J Gordon Millichap
Izdano: (2002-03-01)

Large café-au-lait spots on a 5-year-old boy
od: Brett D. McLarney, PhD, et al.
Izdano: (2022-10-01)

A Baby with Café-au-lait Macules and Aberrant Mongolian Spot: Report of Phakomatosis Pigmentopigmentaria
od: Vishalakshi S Pandit, et al.
Izdano: (2024-07-01)

Characteristics of Café-au-lait Macules and their Association with the Neurofibromatosis type I Genotype in a Cohort of Greek Children
od: Lamprini Nasi, et al.
Izdano: (2023-06-01)

Retinal cafe-au-lait macules: A rare retinal finding in a patient with neurofibromatosis type 1
od: Ramesh Venkatesh, et al.
Izdano: (2019-01-01)

KIT gene mutation causing piebaldism associated with multiple Café Au-Lait like macules and freckling: Delineating a cause of this coexistence
od: Shibhani S Hegde, et al.
Izdano: (2023-01-01)

The treatment of infantile giant café au lait spot using golden parameter therapy with a high fluence 1064-nm Q-switched Nd: YAG laser
od: Hoon Hur, et al.
Izdano: (2024-12-01)

LZTR1 loss-of-function variants associated with café au lait macules with or without freckling
od: Svea Horn, et al.
Izdano: (2024-08-01)

Case report: Gene mutation analysis and skin imaging of isolated café-au-lait macules
od: Zhenyu Zhong, et al.
Izdano: (2023-03-01)

The mystery of brown shawl over back: a rare case of giant plexiform neurofibroma underlying a giant café-au-lait macule
od: Kinjal D Rambhia, et al.
Izdano: (2022-01-01)

Unusual Presentations of Plexiform Neurofibroma: A Series of Three Cases
od: Anurima Nayak, et al.
Izdano: (2024-07-01)

Diagnostic and pathogenetic role of café-au-lait macules in nevoid basal cell carcinoma syndrome
od: Ponti Giovanni, et al.
Izdano: (2012-10-01)

Multiple intraoral neurofibromas: Case report and review of the literature
od: C Krithika, et al.
Izdano: (2009-01-01)

Genome‐wide association study of café‐au‐lait macule number in neurofibromatosis type 1
od: Heejong Sung, et al.
Izdano: (2020-10-01)

Factors affecting clinical phenotype in children with neurofibromatosis type 1
od: Begül Yağcı-küpeli, et al.
Izdano: (2021-06-01)

Type 1 Neurofibromatosis Sans Neurofibroma: A Case Report Emphasizing the Role of Ocular Examination
od: Yogindher Singh, et al.
Izdano: (2024-09-01)

Neurofibromatosis - case presentation
od: Ioan Buraga, et al.
Izdano: (2014-03-01)

Neurofibromatosis de von Recklinghausen: presentación de un caso de neurofibroma vaginal y revisión de la literatura von recklinghausen’s neurofibromatosis: presenting a case of vaginal neurofibroma and literature review
od: Luz Marcela Celis-Amórtegui, et al.
Izdano: (2012-06-01)

Massive Facial Plexiform Neurofibroma: An Unusual Presentation
od: Jasleen kaur, et al.
Izdano: (2024-08-01)

A case report on smear-Positive pulmonary tuberculosis with neurofibromatosis type-1
od: Khushboo Chavda, et al.
Izdano: (2023-01-01)

Epidemiologic Study of Melanocytic Disorders in Hamadan in 2002
od: Abbas Zamanian, et al.
Izdano: (2006-03-01)

Jaffe Lichtenstein Type Polyostotic Fibrous Dysplasia with Unilateral Absent Testis
od: Anand Ramakrishnan, et al.
Izdano: (2018-05-01)

Neurofibromatose type 1 : à propos d´un cas
od: Alae El Bouaychi, et al.
Izdano: (2020-11-01)

Response to Zoledronic Acid Infusion in Children With Fibrous Dysplasia
od: Sujit Kumar Tripathy, et al.
Izdano: (2020-11-01)

Phenotypic Variability and Cutaneous Features in 2 Siblings with Fanconi Anaemia and FANCA Mutation
od: Noor Almaani, et al.
Izdano: (2024-06-01)

Epidemiology and Outcomes of Neurofibromatosis Type 1 (NF-1): Multicenter Tertiary Experience
od: Almuqbil M, et al.
Izdano: (2024-03-01)

Giant plexiform neurofibroma of digital nerves: A case report and review of the literature
od: Bharat B Dogra, et al.
Izdano: (2016-01-01)

Mechanical Ptosis in Neurofibromatosis Type 1 Heralding the Diagnosis of Right Sided Cervical Vagus Nerve Neurofibroma: A Rare Case Report
od: Jyotiranjan Mallick, et al.
Izdano: (2016-06-01)

A non-classic form of McCune Albright syndrome with different presentations and review of the literatures
od: Ali Reza Navabazam, et al.
Izdano: (2021-07-01)

Neurofibrome de l'avant bras: à propos d'un cas
od: Hda Fahim, et al.
Izdano: (2014-05-01)

Abordagem cirúrgica de neurofibroma gigante Surgical correction of a giant neurofibroma
od: Iana Silva Dias, et al.
Izdano: (2012-06-01)

Le Café Maure comme microcosme d’une vie collective et d’une « sociabilité informelle » dans les nouvelles « Au Café » et « Le Compagnon » de Mohammed Dib
od: Arab Hacène
Izdano: (2018-10-01)

Clinical case of family neurofibromatosis type I
od: O. A. Inozemtsova, et al.
Izdano: (2025-01-01)

McCune Albright syndrome: A case report with review of literature
od: Muhammad Haseeb, et al.
Izdano: (2014-01-01)

McCune-Albright syndrome - A case report with transmission electron microscopy
od: Victor Garcia Neto, et al.
Izdano: (2022-02-01)

Segmental neurofibromatosis: A report of a rare case
od: Pratiksha Sonkusale, et al.
Izdano: (2020-01-01)

Facial Neurocutaneous Markers and their Clinical Profile- A Case Series
od: Bibekananda Mukherjee, et al.
Izdano: (2023-05-01)

Becker’s Naevus Syndrome with Breast Aplasia Due to Postzygotic Mutation of ACTB
od: Jeanne Ramspacher, et al.
Izdano: (2022-10-01)

Neurofibromatosis Type 1 and Hypospadias in a Male 46, XY with a Mutation in the NF1 Gene and a Mutation in NR5A1
od: Perafan-Valdes L, et al.
Izdano: (2022-10-01)