Evidence map›Paper›PMID 39385886›Full record

ArticleCureus2024

Patient With Lipoid Proteinosis Presenting With Sudden-Onset Lower Limb Weakness: A Rare Case.

Hassan Mobarak, Sandra El Helou

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In one paragraph

Article in Cureus, 2024. 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

2 authors.

Hassan MobarakPsychiatry and Behavioral Sciences, Lebanese American University School of Medicine, Beirut, LBN.
Sandra El HelouRadiology, Lebanese American University School of Medicine, Beirut, LBN.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lipoid proteinosis (LP), or Urbach-Wiethe disease, is an infrequent autosomal recessive disorder typified by hyaline material deposition in diverse tissues, including the skin, mucous membranes, and internal organs. This case report addresses an unusual presentation of LP in a 25-year-old male, whose initial symptom was sudden-onset left lower limb weakness. This deviation from the typical dermatological and laryngeal manifestations prevalent in LP compels us to consider LP as a potential causative factor in neurological deficits. Physical examination revealed motor weakness in the left lower limb with several dermatological manifestations. Laboratory tests indicated potential thyroid, liver, and urinary tract pathologies. Brain imaging studies revealed bilateral mesial temporal lobe calcifications consistent with LP with associated cortico-subcortical infarcts and hemorrhagic transformation. Additionally, foraminal disc protrusion at L5-S1 in the patient's back MRI suggested nerve compression contributing to limb weakness. This patient's sudden-onset left lower limb weakness accompanied by imaging findings of cortical and subcortical abnormalities aligns with the spectrum of neurological manifestations associated with LP but is less commonly reported. Moreover, the disturbed liver and thyroid blood tests in this patient suggest a potential link between LP and thyroid and liver pathologies, which needs further investigation. This case illustrates that motor weakness, potentially due to cerebral infarcts and intracerebral hemorrhage, is a possible complication of LP. Further research is necessary to confirm and understand the phenomenology of this complication.

Indexed as

acute ischemiact and mri braindermatological manifestationslipoid proteinosis (lp)neurological deficit

Identifiers

PMID39385886
PMCPMC11463906

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