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

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

Εμφάνιση άλλων εκδόσεων (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...

Πλήρης περιγραφή

Λεπτομέρειες βιβλιογραφικής εγγραφής
Κύριοι συγγραφείς:	Anna Claudia Evangelista dos Santos, Benjamin Heck, Beatriz De Camargo, Fernando Regla Vargas
Μορφή:	Άρθρο
Γλώσσα:	English
Έκδοση:	Sociedade Brasileira de Genética 2016-01-01
Σειρά:	Genetics and Molecular Biology
Θέματα:	café-au-lait maculae pediatric solid tumors birth defects nosology
Διαθέσιμο Online:	http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572016005002104&lng=en&tlng=en

Παρόμοια τεκμήρια

Prevalence of Café-au-Lait Spots in children with solid tumors
ανά: Anna Claudia Evangelista dos Santos, κ.ά.
Έκδοση: (2016-05-01)

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

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ανά: Brett D. McLarney, PhD, κ.ά.
Έκδοση: (2022-10-01)

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ανά: Vishalakshi S Pandit, κ.ά.
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ανά: Lamprini Nasi, κ.ά.
Έκδοση: (2023-06-01)

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ανά: Ramesh Venkatesh, κ.ά.
Έκδοση: (2019-01-01)

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ανά: Shibhani S Hegde, κ.ά.
Έκδοση: (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
ανά: Hoon Hur, κ.ά.
Έκδοση: (2024-12-01)

LZTR1 loss-of-function variants associated with café au lait macules with or without freckling
ανά: Svea Horn, κ.ά.
Έκδοση: (2024-08-01)

Case report: Gene mutation analysis and skin imaging of isolated café-au-lait macules
ανά: Zhenyu Zhong, κ.ά.
Έκδοση: (2023-03-01)

The mystery of brown shawl over back: a rare case of giant plexiform neurofibroma underlying a giant café-au-lait macule
ανά: Kinjal D Rambhia, κ.ά.
Έκδοση: (2022-01-01)

Unusual Presentations of Plexiform Neurofibroma: A Series of Three Cases
ανά: Anurima Nayak, κ.ά.
Έκδοση: (2024-07-01)

Diagnostic and pathogenetic role of café-au-lait macules in nevoid basal cell carcinoma syndrome
ανά: Ponti Giovanni, κ.ά.
Έκδοση: (2012-10-01)

Multiple intraoral neurofibromas: Case report and review of the literature
ανά: C Krithika, κ.ά.
Έκδοση: (2009-01-01)

Genome‐wide association study of café‐au‐lait macule number in neurofibromatosis type 1
ανά: Heejong Sung, κ.ά.
Έκδοση: (2020-10-01)

Factors affecting clinical phenotype in children with neurofibromatosis type 1
ανά: Begül Yağcı-küpeli, κ.ά.
Έκδοση: (2021-06-01)

Type 1 Neurofibromatosis Sans Neurofibroma: A Case Report Emphasizing the Role of Ocular Examination
ανά: Yogindher Singh, κ.ά.
Έκδοση: (2024-09-01)

Neurofibromatosis - case presentation
ανά: Ioan Buraga, κ.ά.
Έκδοση: (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
ανά: Luz Marcela Celis-Amórtegui, κ.ά.
Έκδοση: (2012-06-01)

Massive Facial Plexiform Neurofibroma: An Unusual Presentation
ανά: Jasleen kaur, κ.ά.
Έκδοση: (2024-08-01)

A case report on smear-Positive pulmonary tuberculosis with neurofibromatosis type-1
ανά: Khushboo Chavda, κ.ά.
Έκδοση: (2023-01-01)

Epidemiologic Study of Melanocytic Disorders in Hamadan in 2002
ανά: Abbas Zamanian, κ.ά.
Έκδοση: (2006-03-01)

Jaffe Lichtenstein Type Polyostotic Fibrous Dysplasia with Unilateral Absent Testis
ανά: Anand Ramakrishnan, κ.ά.
Έκδοση: (2018-05-01)

Neurofibromatose type 1 : à propos d´un cas
ανά: Alae El Bouaychi, κ.ά.
Έκδοση: (2020-11-01)

Response to Zoledronic Acid Infusion in Children With Fibrous Dysplasia
ανά: Sujit Kumar Tripathy, κ.ά.
Έκδοση: (2020-11-01)

Phenotypic Variability and Cutaneous Features in 2 Siblings with Fanconi Anaemia and FANCA Mutation
ανά: Noor Almaani, κ.ά.
Έκδοση: (2024-06-01)

Epidemiology and Outcomes of Neurofibromatosis Type 1 (NF-1): Multicenter Tertiary Experience
ανά: Almuqbil M, κ.ά.
Έκδοση: (2024-03-01)

Giant plexiform neurofibroma of digital nerves: A case report and review of the literature
ανά: Bharat B Dogra, κ.ά.
Έκδοση: (2016-01-01)

Mechanical Ptosis in Neurofibromatosis Type 1 Heralding the Diagnosis of Right Sided Cervical Vagus Nerve Neurofibroma: A Rare Case Report
ανά: Jyotiranjan Mallick, κ.ά.
Έκδοση: (2016-06-01)

A non-classic form of McCune Albright syndrome with different presentations and review of the literatures
ανά: Ali Reza Navabazam, κ.ά.
Έκδοση: (2021-07-01)

Neurofibrome de l'avant bras: à propos d'un cas
ανά: Hda Fahim, κ.ά.
Έκδοση: (2014-05-01)

Abordagem cirúrgica de neurofibroma gigante Surgical correction of a giant neurofibroma
ανά: Iana Silva Dias, κ.ά.
Έκδοση: (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
ανά: Arab Hacène
Έκδοση: (2018-10-01)

Clinical case of family neurofibromatosis type I
ανά: O. A. Inozemtsova, κ.ά.
Έκδοση: (2025-01-01)

McCune Albright syndrome: A case report with review of literature
ανά: Muhammad Haseeb, κ.ά.
Έκδοση: (2014-01-01)

McCune-Albright syndrome - A case report with transmission electron microscopy
ανά: Victor Garcia Neto, κ.ά.
Έκδοση: (2022-02-01)

Segmental neurofibromatosis: A report of a rare case
ανά: Pratiksha Sonkusale, κ.ά.
Έκδοση: (2020-01-01)

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Έκδοση: (2023-05-01)

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ανά: Jeanne Ramspacher, κ.ά.
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Neurofibromatosis Type 1 and Hypospadias in a Male 46, XY with a Mutation in the NF1 Gene and a Mutation in NR5A1
ανά: Perafan-Valdes L, κ.ά.
Έκδοση: (2022-10-01)