المؤلفون: Pagani K; Department of Dermatology, University of Massachusetts Chan Medical School, Worcester, Massachusetts, USA., Plumptre I; Department of Dermatology, University of Massachusetts Chan Medical School, Worcester, Massachusetts, USA., Amin S; Department of Dermatology, University of Massachusetts Chan Medical School, Worcester, Massachusetts, USA., Lal K; Department of Dermatology, University of Massachusetts Chan Medical School, Worcester, Massachusetts, USA., Wiss K; Department of Dermatology, University of Massachusetts Chan Medical School, Worcester, Massachusetts, USA.; Department of Pediatrics, University of Massachusetts Chan Medical School, Worcester, Massachusetts, USA., Belazarian L; Department of Dermatology, University of Massachusetts Chan Medical School, Worcester, Massachusetts, USA.; Department of Pediatrics, University of Massachusetts Chan Medical School, Worcester, Massachusetts, USA.

المصدر: Pediatric dermatology [Pediatr Dermatol] 2023 May-Jun; Vol. 40 (3), pp. 446-451. Date of Electronic Publication: 2023 Feb 22.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Wiley Country of Publication: United States NLM ID: 8406799 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1525-1470 (Electronic) Linking ISSN: 07368046 NLM ISO Abbreviation: Pediatr Dermatol Subsets: MEDLINE

مواضيع طبية MeSH: Dermatology* , Pigmentation Disorders*/epidemiology , Pigmentation Disorders*/genetics , Neurofibromatosis 1*/diagnosis, Humans ; Female ; Male ; Mosaicism ; Retrospective Studies ; Cafe-au-Lait Spots/epidemiology ; Cafe-au-Lait Spots/genetics ; Cafe-au-Lait Spots/diagnosis

المؤلفون: Blegen K; Department of Pediatrics, Baylor College of Medicine, The Children's Hospital of San Antonio, San Antonio, Texas, USA., Ortiz-Romero SE; Department of Radiology, Baylor College of Medicine, The Children's Hospital of San Antonio, San Antonio, Texas, USA., Juarez O; Department of Genetics, Baylor College of Medicine, The Children's Hospital of San Antonio, San Antonio, Texas, USA., Voeller J; Department of Hematology Oncology, Baylor College of Medicine, The Children's Hospital of San Antonio, San Antonio, Texas, USA.

المصدر: Pediatric dermatology [Pediatr Dermatol] 2022 Sep; Vol. 39 (5), pp. 764-766. Date of Electronic Publication: 2022 Jun 23.

نوع المنشور: Case Reports

بيانات الدورية: Publisher: Wiley Country of Publication: United States NLM ID: 8406799 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1525-1470 (Electronic) Linking ISSN: 07368046 NLM ISO Abbreviation: Pediatr Dermatol Subsets: MEDLINE

مواضيع طبية MeSH: Elephantiasis*/complications , Neurofibroma, Plexiform*/complications , Neurofibroma, Plexiform*/drug therapy , Neurofibromatosis 1*/complications , Neurofibromatosis 1*/drug therapy, Benzimidazoles ; Child ; Female ; Humans ; Mitogen-Activated Protein Kinase Kinases/therapeutic use

المؤلفون: Spurr A; Division of Dermatology, Faculty of Medicine, University of Ottawa, Ottawa, Ontario, Canada., DeBiasio C; Faculty of Medicine, University of Ottawa, Ottawa, Ontario, Canada., El Demellawy D; Department of Pathology, Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada.; University of Ottawa, Ottawa, Ontario, Canada., Gavigan G; Division of Dermatology, Faculty of Medicine, University of Ottawa, Ottawa, Ontario, Canada.; Division of Dermatology, Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada.

المصدر: Pediatric dermatology [Pediatr Dermatol] 2022 Jul; Vol. 39 (4), pp. 664-666. Date of Electronic Publication: 2022 May 03.

نوع المنشور: Case Reports; Journal Article

بيانات الدورية: Publisher: Wiley Country of Publication: United States NLM ID: 8406799 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1525-1470 (Electronic) Linking ISSN: 07368046 NLM ISO Abbreviation: Pediatr Dermatol Subsets: MEDLINE

مواضيع طبية MeSH: Lip Neoplasms*/complications , Lip Neoplasms*/diagnosis , Lip Neoplasms*/pathology , Neurofibromatosis 1*/complications , Neurofibromatosis 1*/diagnosis , Neurofibromatosis 1*/pathology , Rhabdomyosarcoma, Embryonal*/complications , Rhabdomyosarcoma, Embryonal*/diagnosis, Cafe-au-Lait Spots/complications ; Cafe-au-Lait Spots/diagnosis ; Child ; Female ; Humans ; Infant

المؤلفون: Albaghdadi M; Temerty Faculty of Medicine, University of Toronto, Toronto, ON, Canada., Berseneva M; Temerty Faculty of Medicine, University of Toronto, Toronto, ON, Canada., Pennal A; Division of Dermatology, Department of Pediatrics, Hospital for Sick Children, Toronto, ON, Canada., Wan S; Division of Dermatology, Department of Pediatrics, Hospital for Sick Children, Toronto, ON, Canada., Matviychuk D; Division of Clinical and Metabolic Genetics, Hospital for Sick Children, Toronto, ON, Canada.; Department of Paediatric Laboratory Medicine, Hospital for Sick Children, Toronto, ON, Canada., Shugar A; Division of Clinical and Metabolic Genetics, Hospital for Sick Children, Toronto, ON, Canada.; Department of Molecular Genetics, University of Toronto, Toronto, ON, Canada., Kannu P; Department of Medical Genetics, University of Alberta, Edmonton, ON, Canada., Lara-Corrales I; Division of Dermatology, Department of Pediatrics, Hospital for Sick Children, Toronto, ON, Canada.

المصدر: Pediatric dermatology [Pediatr Dermatol] 2022 Mar; Vol. 39 (2), pp. 205-210. Date of Electronic Publication: 2022 Feb 17.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Wiley Country of Publication: United States NLM ID: 8406799 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1525-1470 (Electronic) Linking ISSN: 07368046 NLM ISO Abbreviation: Pediatr Dermatol Subsets: MEDLINE

مواضيع طبية MeSH: Cafe-au-Lait Spots*/complications , Neurofibromatosis 1*/complications , Neurofibromatosis 1*/diagnosis , Neurofibromatosis 1*/genetics, Child ; Child, Preschool ; Female ; Genetic Testing ; Hospitals ; Humans ; Infant ; Male ; Retrospective Studies

المؤلفون: Batalla A; Departments of Dermatology and Pediatrics, Complejo Hospitalario Universitario de Pontevedra, Pontevedra, Spain., Iglesias-Puzas Á; Departments of Dermatology and Pediatrics, Complejo Hospitalario Universitario de Pontevedra, Pontevedra, Spain., Freire-Bruno J; Departments of Dermatology and Pediatrics, Complejo Hospitalario Universitario de Pontevedra, Pontevedra, Spain., Herrero-Hermida J; Departments of Dermatology and Pediatrics, Complejo Hospitalario Universitario de Pontevedra, Pontevedra, Spain., Flórez Á; Departments of Dermatology and Pediatrics, Complejo Hospitalario Universitario de Pontevedra, Pontevedra, Spain.

المصدر: Pediatric dermatology [Pediatr Dermatol] 2018 Sep; Vol. 35 (5), pp. e268-e271. Date of Electronic Publication: 2018 Jul 01.

نوع المنشور: Case Reports; Journal Article

بيانات الدورية: Publisher: Wiley Country of Publication: United States NLM ID: 8406799 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1525-1470 (Electronic) Linking ISSN: 07368046 NLM ISO Abbreviation: Pediatr Dermatol Subsets: MEDLINE

مواضيع طبية MeSH: Neurofibromatosis 1/*genetics , Neurofibromin 1/*genetics, Adolescent ; Adult ; Female ; Genetic Association Studies ; Genotype ; Humans ; Male ; Mutation ; Neurofibromatosis 1/diagnosis ; Phenotype

المؤلفون: Han AM; Division of Pediatric and Adolescent Dermatology, Rady Children's Hospital, San Diego, California.; Departments of Dermatology and Pediatrics, San Diego School of Medicine, University of California, San Diego, California., Kusari A; Division of Pediatric and Adolescent Dermatology, Rady Children's Hospital, San Diego, California.; Departments of Dermatology and Pediatrics, San Diego School of Medicine, University of California, San Diego, California., Soeprono F; Division of Pediatric and Adolescent Dermatology, Rady Children's Hospital, San Diego, California.; Departments of Dermatology and Pediatrics, San Diego School of Medicine, University of California, San Diego, California., Eichenfield LF; Division of Pediatric and Adolescent Dermatology, Rady Children's Hospital, San Diego, California.; Departments of Dermatology and Pediatrics, San Diego School of Medicine, University of California, San Diego, California.

المصدر: Pediatric dermatology [Pediatr Dermatol] 2019 Jul; Vol. 36 (4), pp. e97-e98. Date of Electronic Publication: 2019 May 24.

نوع المنشور: Case Reports; Journal Article; Review

بيانات الدورية: Publisher: Wiley Country of Publication: United States NLM ID: 8406799 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1525-1470 (Electronic) Linking ISSN: 07368046 NLM ISO Abbreviation: Pediatr Dermatol Subsets: MEDLINE

مواضيع طبية MeSH: Abnormalities, Multiple/*diagnosis , Cafe-au-Lait Spots/*diagnosis , Intellectual Disability/*diagnosis , Melanosis/*diagnosis , Neurofibromatosis 1/*diagnosis, Abnormalities, Multiple/genetics ; Adolescent ; Cafe-au-Lait Spots/complications ; Cafe-au-Lait Spots/genetics ; Chromosome Deletion ; Chromosomes, Human, Pair 17/genetics ; Follow-Up Studies ; Genetic Predisposition to Disease ; Humans ; Intellectual Disability/complications ; Intellectual Disability/genetics ; Male ; Melanosis/complications ; Neurofibromatosis 1/complications ; Rare Diseases ; Risk Assessment

SCR Disease Name: Chromosome 17q21.31 Deletion Syndrome

المؤلفون: García-Romero MT; Dermatology Section, Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada.; Department of Pediatric Medicine, Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada., Parkin P; Department of Pediatric Medicine, Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada., Lara-Corrales I; Dermatology Section, Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada.; Department of Pediatric Medicine, Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada.

المصدر: Pediatric dermatology [Pediatr Dermatol] 2016 Jan-Feb; Vol. 33 (1), pp. 9-17. Date of Electronic Publication: 2015 Sep 04.

نوع المنشور: Journal Article; Review; Systematic Review

بيانات الدورية: Publisher: Wiley Country of Publication: United States NLM ID: 8406799 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1525-1470 (Electronic) Linking ISSN: 07368046 NLM ISO Abbreviation: Pediatr Dermatol Subsets: MEDLINE

مواضيع طبية MeSH: Mosaicism*, Neurofibromatosis 1/*diagnosis, Humans ; Neurofibromatosis 1/complications

المؤلفون: Jans SR; Department of Pediatrics, Roskilde Hospital, Roskilde, Denmark., Schomerus E, Bygum A

المصدر: Pediatric dermatology [Pediatr Dermatol] 2015 Jan-Feb; Vol. 32 (1), pp. e29-32. Date of Electronic Publication: 2014 Dec 16.

نوع المنشور: Case Reports; Journal Article

بيانات الدورية: Publisher: Wiley Country of Publication: United States NLM ID: 8406799 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1525-1470 (Electronic) Linking ISSN: 07368046 NLM ISO Abbreviation: Pediatr Dermatol Subsets: MEDLINE

مواضيع طبية MeSH: Leukemia, Myelomonocytic, Juvenile/*diagnosis , Neurofibromatosis 1/*diagnosis , Neurofibromin 1/*genetics , Xanthogranuloma, Juvenile/*diagnosis, Bone Marrow Transplantation ; Drug Therapy ; Early Diagnosis ; Humans ; Infant ; Leukemia, Myelomonocytic, Juvenile/therapy ; Male ; Mutation ; Neurofibromatosis 1/genetics ; Neurofibromatosis 1/therapy ; Treatment Outcome ; Xanthogranuloma, Juvenile/therapy

المؤلفون: Nanda A; Pediatric Dermatology Unit, As'ad Al-Hamad Dermatology Center, Al-Sabah Hospital, Kuwait. artinanda@hotmail.com

المصدر: Pediatric dermatology [Pediatr Dermatol] 2008 May-Jun; Vol. 25 (3), pp. 392-3.

نوع المنشور: Case Reports; Journal Article

بيانات الدورية: Publisher: Wiley Country of Publication: United States NLM ID: 8406799 Publication Model: Print Cited Medium: Internet ISSN: 1525-1470 (Electronic) Linking ISSN: 07368046 NLM ISO Abbreviation: Pediatr Dermatol Subsets: MEDLINE

مواضيع طبية MeSH: Alopecia Areata/*complications , Autoimmune Diseases/*complications , Neurofibromatosis 1/*complications , Thyroiditis, Autoimmune/*complications , Vitiligo/*complications, Alopecia Areata/pathology ; Cafe-au-Lait Spots/pathology ; Child ; Female ; Humans ; Male ; Neurofibromatosis 1/immunology ; Neurofibromatosis 1/pathology ; Scalp/pathology ; Skin/pathology ; Vitiligo/pathology

المؤلفون: Malhotra N; University of Alberta, Edmonton, Alberta, Canada., Levy JMS; University of Alberta, Edmonton, Alberta, Canada., Fiorillo L; University of Alberta, Edmonton, Alberta, Canada.

المصدر: Pediatric dermatology [Pediatr Dermatol] 2019 May; Vol. 36 (3), pp. 360-361. Date of Electronic Publication: 2019 Mar 03.

نوع المنشور: Case Reports; Journal Article

بيانات الدورية: Publisher: Wiley Country of Publication: United States NLM ID: 8406799 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1525-1470 (Electronic) Linking ISSN: 07368046 NLM ISO Abbreviation: Pediatr Dermatol Subsets: MEDLINE

مواضيع طبية MeSH: Immunosuppressive Agents/*therapeutic use , Neurofibroma/*drug therapy , Neurofibromatosis 1/*complications , Sirolimus/*therapeutic use , Skin Neoplasms/*drug therapy, Administration, Cutaneous ; Adolescent ; Humans ; Male ; Neurofibroma/etiology ; Skin Neoplasms/etiology