Evidence map›Paper›PMID 29096685›Full record

ArticleItalian journal of pediatrics2017

Clinical spectrum of woolly hair: indications for cerebral involvement.

Piero Pavone, Raffaele Falsaperla, Massimo Barbagallo, Agata Polizzi, Andrea D Praticò, Martino Ruggieri

Open access · goldAbstract read
In one paragraph

Article in Italian journal of pediatrics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 47% of its field
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

1 citing paper in PubMed, 11 citations in OpenAlex.

  1. Genetic Hair Disorders: A Review.Dermatology and therapy · 2019
    Review
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

6 authors at 4 institutions in 1 country.

Piero PavoneUniversity-Hospital "Policlinico-Vittorio Emanuele," Catania University, Catania, Italy.
Raffaele FalsaperlaUniversity-Hospital "Policlinico-Vittorio Emanuele," Catania University, Catania, Italy.
Massimo BarbagalloUnit of Pediatrics and Pediatrics Emergency, Hospital "G. Garibaldi", Catania, Italy.
Agata PolizziNational Centre for Rare Diseases, Istituto Superiore di Sanità, Rome, Italy.
Andrea D PraticòDepartment of Clinical and Experimental Medicine, Section of Pediatrics and Child Neuropsychiatry, Catania University, Via Santa Sofia 78, 95100, Catania, Italy. terrenere178@alice.it.
Martino RuggieriDepartment of Clinical and Experimental Medicine, Section of Pediatrics and Child Neuropsychiatry, Catania University, Via Santa Sofia 78, 95100, Catania, Italy.
Azienda Ospedaliero-Universitaria Policlinico - Vittorio Emanuele · ITUniversity of Catania · ITIstituto Superiore di Sanità · ITOspedale Garibaldi · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWoolly Hair is an uncommon congenital anomaly of the scalp hair presenting with strongly coiled hair involving a localized area of the scalp or covering the entire side and occurring in non-black people. Isolated or localized wooly hair is usually benign and is not related to other disorders and/or complications. On the contrary, the generalized type may be related to disorders and syndromes affecting heart, cutis, liver and gastrointestinal organs. Among the syndromes presenting with wooly hair, the most known are the Naxos syndrome, the Carvajal-Huerta syndrome, the wooly hair/hypotrichosis, the ectodermal dysplasia-skin fragility, the tricho-hepato-enteric syndrome. CASE PRESENTATION: To our knowledge, no cases of wooly hair syndromes has been associated to neurologic involvement. Among the clinical notes of patients admitted in the Pediatric Units of the Catania University, we have selected four individuals presenting wooly hair, who showed different clinical features and course: case 1 presenting with a localized wooly hair type; case 2, member of a family affected by WH with autosomal dominant inheritance, not associated to complications; case 3, a wooly hair patient who displayed a progressive, severe form of Rasmussen's encephalitis with fatal evolution, and case 4, wooly hair associated to brain malformation and drug-resistant epilepsy.

conclusionsWith this report, we aim to underline the wide spectrum of clinical presentation of individuals with WH and in particular we wish to give an annotation on a possible association of WH with severe neurologic disorders.

Indexed as

Genetic Predisposition to DiseaseCardiomyopathiesCardiomyopathy, DilatedChildChild, PreschoolEncephalitisFemaleHair DiseasesHumansInfantItalyKeratoderma, PalmoplantarMaleMonitoring, PhysiologicPrognosisRare DiseasesEpilepsyGeneralizedLocalizedRasmussen’s encephalopathyWooly hair

Identifiers

PMID29096685
PMCPMC5667512
OpenAlexW2766383307

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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 OpenQuestion graph.