Evidence map›Paper›PMID 42725218›Full record

ArticleAnnals of medicine and surgery (2012)2026

Phenotypic discordance in semilobar holoprosencephaly: a case report of total arhinia and median clefting linked to gestational diabetes.

Janu Chhetri, Rejina Chhetri

Abstract readCase Reports
In one paragraph

Article in Annals of medicine and surgery (2012), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

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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

2 authors.

Janu ChhetriDepartment of Diagnostic Radiology and Imaging, Fatima Jinnah Medical University, Lahore, Pakistan.
Rejina ChhetriDepartment of Pediatric Surgery, Nepalgunj Medical College, Nepalgunj, Nepal.ORCID https://orcid.org/0009-0002-2253-783X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Holoprosencephaly (HPE) is a complex spectrum of cephalic malformations resulting from incomplete prosencephalic division. Semilobar HPE is an intermediate variant, often associated with significant craniofacial dysmorphism and neurological morbidity. Case presentation: We present a preterm female infant born to a mother with unmanaged gestational diabetes. At birth, she exhibited microcephaly, total arhinia, and a median cleft lip and palate. MRI confirmed semilobar HPE. Clinical progression included hypotonia, seizures, and recurrent hyperpyrexia associated with hypothalamic dysfunction. Despite the absence of a nasal airway, the infant transitioned to reflexive mouth breathing and required long-term orogastric tube feeding. Notably, she has maintained systemic stability throughout an 8-month follow-up, facilitated by a proactive, multidisciplinary home-based care model. Discussion: This case illustrates a phenotypic discordance in which severe arhinia occurs alongside intermediate cerebral cleavage, suggesting a potential vulnerability in which nasal placode development may be highly sensitive to maternal hyperglycemia, which is hypothesized to perturb cholesterol-dependent Sonic Hedgehog signaling. Our clinical experience demonstrates that by prioritizing rigorous caloric titration and proactive monitoring of autonomic and infectious triggers, it is possible to successfully navigate the patient's precarious equilibrium and prevent the secondary morbidity typically associated with hypothalamic instability. Conclusion: This report demonstrates that even in the presence of profound structural and autonomic vulnerabilities, proactive multidisciplinary management can effectively mitigate secondary systemic morbidity and support survival beyond the neonatal period. This approach provides a viable model for stabilizing patients with severe holoprosencephaly through consistent, home-based surveillance and functional support.

Indexed as

arhiniacase reportgestational diabetesneonatal seizuressemilobar holoprosencephalySonic hedgehog signaling

Identifiers

PMID42725218
PMCPMC13561267

What Socratic holds

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Registered trials

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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 Socratic graph.