Evidence map›Paper›PMID 42597118›Full record

ArticleFrontiers in endocrinology2026

Neonatal hypocalcemia and hydrocephalus as early manifestations of intermediate osteopetrosis: successful hematopoietic stem cell transplantation despite negative genetic testing: a case report.

Laura Figà, Daniele Franzone, Maura Faraci, Filomena Pierri, Sara Pestarino, Giulia Amico, Francesca Faravelli, Gianluca Piatelli, Anna Elsa Maria Allegri, Mohamad Maghnie and 2 more

Abstract readCase Reports
In one paragraph

Article in Frontiers in endocrinology, 2026. 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
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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

12 authors.

Laura FigàDepartment of Neuroscience, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health (DINOGMI), University of Genoa, Genoa, Italy.
Daniele FranzonePediatrics and Neonatology Unit of Savona, IRCCS Istituto Giannina Gaslini, Genoa, Italy.
Maura FaraciHematopoietic Stem Cell Transplantation Unit, IRCCS Istituto G. Gaslini, Genova, Italy.
Filomena PierriHematopoietic Stem Cell Transplantation Unit, IRCCS Istituto G. Gaslini, Genova, Italy.
Sara PestarinoHematopoietic Stem Cell Transplantation Unit, IRCCS Istituto G. Gaslini, Genova, Italy.
Giulia AmicoLaboratory of Human Genetics, IRCCS Istituto Giannina Gaslini, Genoa, Italy.
Francesca FaravelliGenomics and Clinical Genetics Unit, IRCCS Istituto Giannina Gaslini, Genova, Italy.
Gianluca PiatelliNeurosurgery Unit, IRCCS Istituto Giannina Gaslini, Genova, Italy.
Anna Elsa Maria AllegriPaediatric Endocrinology Unit, Department of Paediatrics, IRCCS Istituto Giannina Gaslini, Genoa, Italy.
Mohamad MaghnieDepartment of Neuroscience, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health (DINOGMI), University of Genoa, Genoa, Italy.
Flavia NapoliPaediatric Endocrinology Unit, Department of Paediatrics, IRCCS Istituto Giannina Gaslini, Genoa, Italy.
Natascia di IorgiDepartment of Neuroscience, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health (DINOGMI), University of Genoa, Genoa, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Osteopetrosis is a rare genetic skeletal disorder caused by defective osteoclast-mediated bone resorption, leading to increased bone density and complications including hypocalcemia, pancytopenia, cranial nerve compression, and, more rarely, hydrocephalus. We report a rare case of intermediate osteopetrosis presenting with neonatal hypocalcemia and progressive macrocephaly. Brain magnetic resonance imaging confirmed obstructive hydrocephalus, which was treated with ventriculoperitoneal shunting. Clinical and radiological findings supported the diagnosis of osteopetrosis, although targeted genetic testing and whole exome sequencing did not identify a causative variant. The patient was treated with calcium gluconate and vitamin D supplementation, followed by hematopoietic stem cell transplantation from an HLA-matched unrelated donor using peripheral blood stem cells. This case highlights the importance of early recognition and timely hematopoietic stem cell transplantation to promote successful engraftment and improve long-term outcomes, even in the absence of molecular confirmation.

Indexed as

Hematopoietic Stem Cell TransplantationHydrocephalusHypocalcemiaOsteopetrosisChildChild, PreschoolFemaleGenetic TestingHumansInfantInfant, NewbornMalecase reporthematopoietic stem-cell transplantationhydrocephalushypocalcaemiaosteopetrosis

Identifiers

PMID42597118
PMCPMC13467747

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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.