Cargando…

Hypomelanosis of Ito with Multiple Congenital Anomalies

Hypomelanosis of Ito (HI) is a neurocutaneous disorder, also known as incontinentia pigmenti achromians. HI has been associated with chromosomal abnormalities, especially mosaicism. Herein, we report a case of HI with multiple congenital anomalies. A 2-month-old girl presented with multiple linear a...

Descripción completa

Detalles Bibliográficos
Autores principales:	Yu, Da-Ae, Kwon, Ohsang, Kim, Kyu Han
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	The Korean Dermatological Association; The Korean Society for Investigative Dermatology 2019
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7992565/ https://www.ncbi.nlm.nih.gov/pubmed/33911653 http://dx.doi.org/10.5021/ad.2019.31.5.576

Ejemplares similares

HYPOMELANOSIS OF ITO: A CASE REPORT
por: Gupta, Monisha, et al.
Publicado: (2002)

Hypomelanosis of Ito with an unusual pulmonary abnormality in an infant
por: Bhat, Ramesh Y., et al.
Publicado: (2014)

An Interesting Coexistence of Multifocal Hypertrichosis and Hirsutism in Hypomelanosis of Ito
por: Mendiratta, Vibhu, et al.
Publicado: (2019)

Possible Correlation between Hypomelanosis of Ito and Wilms' Tumor
por: Bello-Germino, Daniella, et al.
Publicado: (2018)

Hypomelanosis of Ito presenting with pediatric orthopedic issues: a case report
por: Trägårdh, Malene, et al.
Publicado: (2014)

Hypomelanosis of Ito with a trisomy 2 mosaicism: a case report
por: Ponti, Giovanni, et al.
Publicado: (2014)

Retinoblastoma Presenting in a Child with Hypomelanosis of Ito
por: El-Sawy, Tarek, et al.
Publicado: (2011)

A case of hypomelanosis of Ito accompanied by unilateral abnormal limb overgrowth and delayed speech
por: Ozcetin, Mustafa, et al.
Publicado: (2018)

Clinical spectrum of MTOR-related hypomelanosis of Ito with neurodevelopmental abnormalities
por: Carmignac, Virginie, et al.
Publicado: (2021)

Total Hemi-overgrowth in Pigmentary Mosaicism of the (Hypomelanosis of) Ito Type: Eight Case Reports
por: Pavone, Vito, et al.
Publicado: (2016)

Acral speckled hypomelanosis
por: Aldhalaan, Jumana, et al.
Publicado: (2019)

Total Hemi-overgrowth in Pigmentary Mosaicism of the (Hypomelanosis of) Ito Type: Eight Case Reports: Erratum
Publicado: (2016)

Successful treatment of progressive macular hypomelanosis
por: Leonard, Nicholas, et al.
Publicado: (2020)

Transient cutaneous hypomelanosis after cryoanesthesia
por: Pippi, Roberto, et al.
Publicado: (2022)

Progressive Macular Hypomelanosis: A Rarely Diagnosed Hypopigmentation in Caucasians
por: Neynaber, Sven, et al.
Publicado: (2009)

Idiopathic Guttate Hypomelanosis Treated with 308-nm Excimer Light and Topical Bimatoprost
por: Kreeshan, Firas Constantin, et al.
Publicado: (2021)

Vulvar vitiligo-like depigmentation and multiple halos of hypomelanosis at the trunk following treatment with imiquimod 5% cream for vulvar condylomata: casual or related events?
por: Serra, Maíra Chiarelli, et al.
Publicado: (2014)

Therapeutic wounding - 88% phenol in idiopathic guttate hypomelanosis
por: Ravikiran, Shilpashree P., et al.
Publicado: (2014)

Incomplete bladder duplication with multiple congenital anomalies: A rare presentation
por: Awasthi, Nipun Kumar, et al.
Publicado: (2015)

Anaesthetic Management of A Child with Multiple Congenital Anomalies Scheduled for Cataract Extraction
por: Kulkarni, Kalpana, et al.
Publicado: (2009)

Congenital fusion of jaw and ankyloblepharon filiforme adnatum: Malformation and multiple systems anomaly
por: Reddy, Mallika P, et al.
Publicado: (2012)

A case of incomplete duplication of the portal vein associated with multiple congenital anomalies
por: Ichikawa, Tamaki, et al.
Publicado: (2023)

Mosaic Ring Chromosome 6 in an Infant with Significant Patent Ductus Arteriosus and Multiple Congenital Anomalies
por: Lee, Seung Jae, et al.
Publicado: (2012)

Dermoscopic evaluation of idiopathic guttate hypomelanosis: A preliminary observation
por: Ankad, Balachandra S., et al.
Publicado: (2015)

Scrotoschisis: An extremely rare congenital anomaly
por: Shukla, Ram M., et al.
Publicado: (2012)

Congenital Skull Anomaly with Multiple Brain Stones and Symptomatic Meningioma of Medial Sphenoid Wing
por: Chaturvedi, Monali, et al.
Publicado: (2018)

Congenital Ocular Anomaly in an Infant with Trisomy 14 Mosaicism
por: Choi, Jun Ho, et al.
Publicado: (2012)

Clinical Features and Surgical Results in Harada-Ito Surgery Patients
por: Ayyıldız, Önder, et al.
Publicado: (2018)

Progressive macular hypomelanosis among Egyptian patients: a clinicopathological study
por: Selim, Mohamed Khaled, et al.
Publicado: (2011)

Propionibacterium Acnes Phylogenetic Type III is Associated with Progressive Macular Hypomelanosis
por: Petersen, Rolf L. W., et al.
Publicado: (2017)

Acquired Speckled Acrofacial Hypomelanosis: A Novel Presentation of an Existing Dermatosis
por: Singh, Ajeet, et al.
Publicado: (2022)

Fetus-in-fetu: A Rare Congenital Anomaly
por: Gupta, Saurabh Kumar, et al.
Publicado: (2010)

Pentalogy of Cantrell: An Extremely Rare Congenital Anomaly
por: Chandran, Suresh, et al.
Publicado: (2013)

Poland syndrome a rare congenital anomaly
por: Ibrahim, Aliyu, et al.
Publicado: (2013)

Cyclopia with proboscis: A rare congenital anomaly
por: Kunwar, Asma, et al.
Publicado: (2021)

Novel Hypomorphic Mutation in FANCD2 Gene Observed in a Fetus with Multiple Congenital Anomalies
por: Vazharova, Radoslava, et al.
Publicado: (2016)

PIGN mutation multiple congenital anomalies-hypotonia-seizures syndrome 1: A case report
por: Hou, Fei, et al.
Publicado: (2022)

Toyo Ito
por: Ito, Toyoo, 1941-
Publicado: (2009)

Concurrent pulmonary hypoplasia and congenital lobar emphysema in a young dog with tension pneumothorax: a rare congenital pulmonary anomaly
por: Han, Hyun-Jung, et al.
Publicado: (2019)

Near infrared photothermoelectric effect in transparent AZO/ITO/Ag/ITO thin films
por: Bianchi, C., et al.
Publicado: (2021)

Cannot write session to /tmp/vufind_sessions/sess_qo3n85copa29quu2ab7phtfuib