Evidence map›Paper›PMID 29704303›Full record

ArticleAmerican journal of medical genetics. Part A2018

Atypical presentations associated with non-polyalanine repeat PHOX2B mutations.

Umakanth Katwa, Alissa M D'Gama, Anita E Qualls, Lucas M Donovan, Jody Heffernan, Jiahai Shi, Pankaj B Agrawal

Open access · greenAbstract readCase Reports
In one paragraph

Article in American journal of medical genetics. Part A, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.7field-weighted citation impact, top 34% 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

6 citing papers in PubMed, 13 citations in OpenAlex.

  1. Children (Basel, Switzerland) · 2026
    Article
  2. Article
  3. Article
  4. Case Report: A novelFrontiers in pediatrics · 2022
    Article
  5. Article
  6. Article
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

7 authors at 2 institutions in 2 countries.

Umakanth KatwaDivision of Pulmonology, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts.
Alissa M D'GamaDivision of Genetics and Genomics, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts.ORCID http://orcid.org/0000-0002-2482-5328
Anita E QuallsDivision of Newborn Medicine, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts.
Lucas M DonovanDivision of Pulmonology, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts.
Jody HeffernanDivision of Newborn Medicine, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts.
Jiahai ShiDepartment of Biomedical Sciences, City University of Hong Kong, Hong Kong SAR, China.
Pankaj B AgrawalDivision of Genetics and Genomics, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts.
Boston Children's Hospital · USCity University of Hong Kong · HK

Funding

Medical Scientist Training ProgramT32GM007753 · NIGMS · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI WALENSKY, LOREN DAVID · 1985 to 2021
$50.0M
Genome Sequence-Based Screening for Childhood Risk and Newborn IllnessU19HD077671 · NICHD · BRIGHAM AND WOMEN'S HOSPITAL · PI BEGGS, ALAN H., GREEN, ROBERT C. · 2013 to 2018
$6.1M
SPEG is Critical in Skeletal Muscle Development and FunctionR01AR068429 · NIAMS · BOSTON CHILDREN'S HOSPITAL · PI AGRAWAL, PANKAJ B · 2015 to 2019
$1.9M
NIAMS NIH HHS R01 AR068429NICHD NIH HHS U19 HD077671NIGMS NIH HHS T32 GM007753
6 · The paper itself

Abstract

Congenital central hypoventilation syndrome (CCHS) is a disorder of ventilatory control and autonomic dysregulation that can be caused by mutations in the paired-like homeobox 2B (PHOX2B) gene. The majority of CCHS cases are caused by polyalanine repeat mutations (PARMs) in PHOX2B; however, in rare cases, non-polyalanine repeat mutations (NPARMs) have been identified. Here, we report two patients with NPARMs in PHOX2B. Patient 1 has a mild CCHS phenotype seen only on polysomnogram, which was performed for desaturations and stridor following a bronchiolitis episode, and characterized by night-time hypoventilation and a history of ganglioneuroblastoma. She carried a novel de novo missense variant, p.R102S (c.304C > A), in exon 2. Patient 2 has an atypical CCHS phenotype including micrognathia, gastroesophageal reflux, stridor, hypopnea, and intermittent desaturations. Sleep study demonstrated that Patient 2 had daytime and night-time hypercarbia with obstructive sleep apnea, requiring tracheostomy. On PHOX2B sequencing, she carried a recently identified nonsense variant, p.Y78* (c.234C > G), in exon 1. In summary, we present two patients with CCHS and identified NPARMs in PHOX2B who have distinct differences in phenotype severity, further elucidating the range of clinical outcomes in CCHS and illustrating the necessity of considering PHOX2B mutations when encountering atypical CCHS presentations.

Indexed as

MutationChild, PreschoolFemaleHomeodomain ProteinsHumansHypoventilationInfant, NewbornPhenotypePrognosisSleep Apnea, CentralTranscription FactorsHomeodomain ProteinsNBPhox proteinTranscription Factorscongenital central hypoventilation syndromeneuroblastomaneurocristopathynon-polyalanine repeat mutationsPHOX2B

Identifiers

PMID29704303
PMCPMC6117218
OpenAlexW2801852435

What OpenQuestion holds

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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.