Results 61 to 70 of about 762 (161)

Pediatric Interventions in a Sanfilippo Syndrome Patient Under General Anesthesia: A Case Report

Case Reports in Dentistry, Volume 2025, Issue 1, 2025.
Background: Mucopolysaccharidosis (MPS) Type III (MPS III) or Sanfilippo syndrome is a rare autosomal recessive inherited metabolic disorder. This disorder is responsible for lysosomal storage disorder at the cellular aspect. Due to lysosomal enzyme perturbance leading to the alteration of macromolecule metabolisms, this cellular perturbance causes ...
Ahmad Al Malak, Hassan Issawi, Mohammad Hassoun, Mohammad Al Halabi, Darko Macan   +4 more
wiley   +1 more source

Evaluation of Efficacy of 1064 nm Q Switched Nd:YAG Laser Treatment in the Nevus of Ota: Seven-year Retrospective Study

Journal of Dermatology and Dermatologic Surgery
Background: Nevus of Ota is a benign skin condition characterized by dermal melanocytosis. Q switched Nd:YAG laser (QSNYL) has become the mainstay of therapy for treating this condition probably because of the minimum side effects and their noninvasive ...
Neenu Kaul, Neeti Kumari, Shiv D. S. Rawat   +2 more
doaj   +1 more source

On the Extracellular Sheath of Dermal Melanocytes in Nevus Fuscocereleus Acromiodeltoideus (Ito) and Mongolian Spot. An Ultrastructural Study

, 1979
The dermal melanocytes in the lesions of nevus of Ito and Mongolian spot were shown to possess the extracellular sheath composed of both fine filaments and granules (2–5nm in diameter).
Okawa, Yokon, Yokota, Reiko, Yamauchi, Akio   +2 more
core   +1 more source

Red-white and blue baby: a case of phacomatosis pigmentovascularis type V [PDF]

, 2015
Phacomatosis pigmentovascularis is a rare genodermatosis characterized by the combination of an extensive pigmentary nevus with a widespread vascular nevus.
Yoong, Corinne, Zappala, Tania, Byrom, Lisa, Surjana, Devita   +3 more
core   +1 more source

Dermatological changes in a prospective cohort of acutely ill, hospitalised Malawian children, stratified according to nutritional status

BMJ Paediatrics Open
Rationale Since the first documentation of skin changes in malnutrition in the early 18th century, various hair and skin changes have been reported in severely malnourished children globally.
Michael Boele van Hensbroek, Robert H J Bandsma, Debbie Thompson, Judd L Walson, Kelvin Mponda, Wieger Voskuijl, Emmie Mbale, Deborah van den Brink, Colette van Hees, Fletchter Ngong'a, Emma Segula, Daniella Brals, James Berkely   +12 more
doaj   +1 more source

Beyond an Extensive Dermal Melanocytosis: A Case of Phacomatosis Pigmentovascularis of Cesioflammea Type

Portuguese Journal of Pediatrics, 2023
Bárbara Aguiar, Inês Vidreiro, Margarida Valente, Hugo Cavaco   +3 more
doaj   +1 more source

Imatinib Mesylate-Induced Acquired Dermal Melanocytosis and Acquired Bilateral Nevus of Ota-Like Macules. [PDF]

Ann Dermatol, 2021
Jang JW, Song CH, Jung YJ, Cheon DU, Koh WS, Ro YS, Ko JY.   +6 more
europepmc   +1 more source

Nevus of Ota Associated with Nevus of Ito : A Rare Case Report

JK Science
Except for the difference in distribution, Nevus of Ito and Nevus of Ota are very similar. In this report, we present the rare simultaneous occurrence of Nevus of Ota and Nevus of Ito in a21-year-old female patient.
Noel Sam Thomas, Neha Mariam Joseph
doaj  

Phagocytosis and Degradation of Melanosomes by the Mast Cells**From the Department of Dermatology, Sapporo Medical College, Sapporo, Japan.

, 1969
In this electron microscopic study, the melanosomes were always seen as degradative conglomerates within phagocytic vacuoles of the mast cells of skin lesions of dermal melanocytosis and blue nevus.
Kukita, Atsushi, Sato, Syozo, Atsushi Kukita, Sato, Shin-ichi, Shin-ichi Sato, Syozo Sato   +5 more
core   +1 more source

Gene discovery in extensive dermal melanocytosis reveals multiple mosaic causes

BACKGROUND: Extensive and/or atypical dermal melanocytosis (EDM) is abnormal macular blue/black skin pigmentation which can be associated with other congenital abnormalities and an increased risk of melanoma. It is likely underdiagnosed due to phenotypic
Polubothu, Satyamaanasa, Zecchin, Davide, O'Neil, Claire, Henderson, Robert A, Dyankova-Peeva, Daniela, Izadi, Fereshteh, Kinsler, Veronica A, Sauvadet, Aimie, Barberan-Martin, Sara, Laskar, Rezwanuzzaman, Cullup, Thomas, Lomas, Debra, Knöpfel, Nicole, Del Valle Torres, Ignacio, Bryant, Dale, Macrae, Frances   +15 more
core