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ALLMedicine™ Incontinentia Pigmenti Center

Research & Reviews  114 results

Incontinentia Pigmenti: X-Linked Skin Disorder: A Case Report.
https://doi.org/10.1891/11-T-725
Neonatal Network : NN; Gelardi L

Mar 10th, 2022 - Incontinentia pigmenti (IP) is a rare X-linked neuroectodermal dysplasia affecting the skin, hair, teeth, nails, microvasculature, and central nervous system. Mutations in the IKBKG gene cause this disorder. Incontinentia pigmenti is found in 65-7...

The Forgotten Phacomatoses: A Neuroimaging Review of Rare Neurocutaneous Disorders.
https://doi.org/10.1067/j.cpradiol.2021.07.002
Current Problems in Diagnostic Radiology; Samara A, Gusman M et. al.

Oct 6th, 2021 - Phakomatoses, or neurocutaneous syndromes, are a heterogeneous group of rare genetic disorders that predominantly affect structures arising from the embryonic ectoderm, namely the skin, eye globe, retina, tooth enamel, and central nervous system. ...

The Anesthetic Challenges of Caring for a Pediatric Patient With Incontinentia Pigmenti...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7846286
A&A Practice; Baig SM, Pandya Shah S

May 15th, 2021 - Incontinentia pigmenti (IP) is a rare X-linked dominant disorder. We present a case of an infant with IP who was brought to the operating room for panretinal diode photocoagulation under general anesthesia. The anesthesia team was unable to obtain...

Development of dentofacial characteristics related to Incontinentia Pigmenti syndrome: ...
https://doi.org/10.1016/j.ajodo.2020.03.033
American Journal of Orthodontics and Dentofacial Orthoped... Santa Maria FD, Barros SE et. al.

Apr 29th, 2021 - This research aimed to investigate the dentofacial characteristics of patients with Incontinentia Pigmenti (IP) (or Bloch-Sulzberger) syndrome in childhood, juvenile, and adulthood developmental stages. Fifteen female patients with a clinical diag...

Pediatric Hypomelanosis of Ito
http://emedicine.medscape.com/article/909996-overview

Apr 12th, 2021 - Background Hypomelanosis of Ito (HI) syndrome is characterized by the presence of whirled hypochromic skin lesions (see the image below) often associated with systemic manifestations. Ito first introduced the syndrome 1951. [1] In 1967, Hamada et ...

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News  8 results

A 6-year-old, otherwise-healthy male is brought into clinic for evaluation of papules on his neck. The rash has been present since 1 year of age and has been growing in size proportionately.
http://www.mdedge.com/pediatrics/article/191029/dermatology/what-your-diagnosis
Anshika Kaushik, MD, Lawrence F. Eichenfield, MD

Dec 12th, 2018 - Epidermal nevi are a subset of cutaneous hamartomas resulting from somatic mutations of epidermal cells, presenting as keratinocyte or epidermal appendage overgrowths. The most common type appear in a linear distribution and are termed linear epid.

A 6-year-old, otherwise-healthy male is brought into clinic for evaluation of papules on his neck. The rash has been present since 1 year of age and has been growing in size proportionately.
https://www.mdedge.com/pediatrics/article/191029/dermatology/what-your-diagnosis
Anshika Kaushik, MD, Lawrence F. Eichenfield, MD

Dec 12th, 2018 - Epidermal nevi are a subset of cutaneous hamartomas resulting from somatic mutations of epidermal cells, presenting as keratinocyte or epidermal appendage overgrowths. The most common type appear in a linear distribution and are termed linear epid.

Three steps are involved in assessing a vesiculopustular lesion
https://www.mdedge.com/clinicianreviews/article/173119/dermatology/three-steps-are-involved-assessing-vesiculopustular
Doug Brunk

Aug 21st, 2018 - LAKE TAHOE, CALIF. – Evaluation of an infant with a vesiculopustular lesion entails a pragmatic approach, with three assessment steps, according to pediatric dermatologist Lawrence A.

Linear Porokeratosis Associated With Multiple Squamous Cell Carcinomas
https://www.mdedge.com/dermatology/article/152458/nonmelanoma-skin-cancer/linear-porokeratosis-associated-multiple-squamous
Blake Friedman, BA, Kseniya Golubets, MD et. al.

Nov 20th, 2017 - Lesions of porokeratosis are thought to arise from disordered keratinization, though the exact pathogenesis remains uncertain. At least 5 clinical subtypes of porokeratosis have been identified: porokeratosis of Mibelli, disseminated superficial p.

Bullous Lesions in a Neonate
https://www.mdedge.com/dermatology/article/145001/pigmentation-disorders/bullous-lesions-neonate
Thomas F. Byrd IV, MD, Samantha Bapty, MD et. al.

Aug 21st, 2017 - The Diagnosis: Incontinentia Pigmenti The infant's mother was noted to have diffuse hypopigmented patches over the trunk, arms, and legs (present since adolescence) with whorled cicatricial alopecia of the vertex scalp and peg-shaped teeth (Figure.

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