scholarly journals Griscelli Syndrome Type 3: A Case Report

2020 ◽  
Vol 08 (06) ◽  
Author(s):  
Shikha Verma ◽  
Keyword(s):  
Case Report ◽  
Syndrome Type ◽  
Griscelli Syndrome ◽  
Type 3

Silvery hair with dyschromatosis: Griscelli syndrome type 3 or familial gigantic melanocytosis

2018 ◽  
Vol 45 (12) ◽  
pp. 918-922
Author(s):  
Meenakshi Batrani ◽  
Akhilesh Thole ◽  
Asha Kubba ◽  
Khushbu Mahajan
Keyword(s):  
Syndrome Type ◽  
Griscelli Syndrome ◽  
Type 3

scholarly journals Griscelli syndrome Type 3 in three non-identical siblings

2021 ◽  
Vol 26 (1) ◽  
pp. 63
Author(s):  
Somya Sharma ◽  
VivekKumar Dey ◽  
Animesh Saxena ◽  
Anil Gour
Keyword(s):  
Syndrome Type ◽  
Griscelli Syndrome ◽  
Type 3

scholarly journals A rare pigmentary disorder in two non-identical siblings: Griscelli Syndrome –type 3

2014 ◽  
Vol 20 (7) ◽  
Author(s):  
Sarabjit Kaur ◽  
Nidhi Jindal ◽  
Surabhi Dayal ◽  
Vijay Kumar Jain ◽  
Vijayeeta Jairath ◽  
...  
Keyword(s):  
Syndrome Type ◽  
Pigmentary Disorder ◽  
Griscelli Syndrome ◽  
Type 3

Pfeiffer Syndrome Type 3 and Prune Belly Anomaly in a Female: Case Report and Review

2019 ◽  
Vol 38 (5) ◽  
pp. 412-417
Author(s):  
Christian Peña-Padilla ◽  
Lorena Viramontes-Aguilar ◽  
Gerónimo Tavares-Macías ◽  
Lucina Bobadilla-Morales ◽  
Michael L. Cunningham ◽  
...  
Keyword(s):  
Case Report ◽  
Syndrome Type ◽  
Pfeiffer Syndrome ◽  
Prune Belly ◽  
Female Case ◽  
Type 3

Griscelli syndrome type 3 in Ethiopian sisters resulting from a homozygous missense mutation in MLPH

2019 ◽  
Vol 59 (3) ◽  
Author(s):  
Kidist Y. Dagnewu ◽  
Adane Ayele ◽  
Lu Liu ◽  
Rashida Pramanik ◽  
Alexandros Onoufriadis ◽  
...  
Keyword(s):  
Missense Mutation ◽  
Syndrome Type ◽  
Homozygous Missense Mutation ◽  
Griscelli Syndrome ◽  
Type 3

scholarly journals Griscelli syndrome-type 2 in twin siblings: case report and update on RAB27A human mutations and gene structure

2008 ◽  
Vol 41 (10) ◽  
pp. 839-848 ◽  
Author(s):  
I.P. Meschede ◽  
T.O. Santos ◽  
T.C. Izidoro-Toledo ◽  
J. Gurgel-Gianetti ◽  
E.M. Espreafico
Keyword(s):  
Case Report ◽  
Gene Structure ◽  
Syndrome Type ◽  
Griscelli Syndrome

scholarly journals Griscelli syndrome type 3 with coexistent universal dyschromia—An uncommon association of a rare entity

2020 ◽  
Vol 11 (5) ◽  
pp. 799
Author(s):  
Surabhi Sinha ◽  
SinuRose Mathachan ◽  
Purnima Malhotra
Keyword(s):  
Syndrome Type ◽  
Rare Entity ◽  
Griscelli Syndrome ◽  
Type 3
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