Evidence map›Paper›PMID 41782981›Full record

ArticleJNMA; journal of the Nepal Medical Association2025

Griscelli Syndrome in Two Siblings with Silvery Hair: A Case Report.

Hanniyah Khwaja, A R Rajan, Nitin Lingayat, Shweta Dhasal

Abstract readCase Reports
In one paragraph

Article in JNMA; journal of the Nepal Medical Association, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Hanniyah KhwajaSymbiosis Medical College for Women & Symbiosis University Hospital & Research Centre, Symbiosis International (Deemed University), Pune, India.
A R RajanDepartment of Paediatrics, Symbiosis Medical College for Women & Symbiosis University Hospital & Research Centre, Symbiosis International (Deemed University), Pune, India.
Nitin LingayatDepartment of Paediatrics, Symbiosis Medical College for Women & Symbiosis University Hospital & Research Centre, Symbiosis International (Deemed University), Pune, India.
Shweta DhasalDepartment of Paediatrics, Symbiosis Medical College for Women & Symbiosis University Hospital & Research Centre, Symbiosis International (Deemed University), Pune, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Griscelli syndrome (GS) is an uncommon disorder characterized by partial albinism, which gives hair a silvery-grey sheen and variable immunodeficiency or neurological impairment, with pancytopenia, immune dysfunction, hepatosplenomegaly, neurological impairment, hypogammaglobulinemia, and variable cellular immunodeficiency. Three variants GS1, GS2 and GS3 have been described in different phenotypes of the disease with varying presentation. We present two neonates, born two years apart, to parents with third-degree consanguinity. Both had features of partial albinism and neutropenia at birth. Microscopy of hair showed characteristic large aggregates of pigment granules dispersed irregularly along the hair shaft. Given their family history and high clinical suspicion, a diagnosis of Griscelli syndrome was made. Early diagnosis of Griscelli syndrome can offer treatment options like Bone Marrow Transplant and prevent fatal complications like hemophagocytic lymphohistiocytosis. Supportive management during transplantation comprises of antimicrobial therapy, immunoglobulin replacement, and vigilant monitoring for complications like graft versus host disease.

Indexed as

HairImmunologic Deficiency SyndromesLymphohistiocytosis, HemophagocyticPiebaldismConsanguinityFemaleHearing Loss, SensorineuralHumansInfant, NewbornMalePigmentation DisordersSiblingsalbinismclumpedmelanosomesgriscelli syndromelymphohiSiocytosis

Identifiers

PMID41782981
PMCPMC12906737

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.