Evidence map›Paper›PMID 36928758›Full record

ReviewEuropean journal of pediatrics2023

Aromatic L-amino acid decarboxylase deficiency in countries in the Middle East: a case series and literature review.

Musaad Abukhaled, Mohammed Al Muqbil, Malak Ali Alghamdi, Khalid Hundallah, Jehan Suleiman, Tawfeg Ben-Omran, Majid Alfadhel, Mohammed Almannai, Rehab Alsaleh, Brahim Tabarki

Erratum issuedOpen access · hybridAbstract readReview
In one paragraph

Review in European journal of pediatrics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.4field-weighted citation impact, top 41% 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, 2 citations in OpenAlex.

  1. Current clinical applications of AAV-mediated gene therapy.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 6 institutions in 3 countries.

Musaad AbukhaledDepartment of Neurosciences, King Faisal Specialist Hospital and Research Center, (KFSH-RC), Riyadh, Saudi Arabia. abukhaled_md@hotmail.com.
Mohammed Al MuqbilCollege of Medicine, King Saud bin Abdulaziz University for Health Sciences (KSAU-HS), Riyadh, Saudi Arabia.
Malak Ali AlghamdiMedical Genetic Division, Pediatric Department, College of Medicine, King Saud University, Riyadh, Saudi Arabia.
Khalid HundallahDivision of Neurology, Department of Pediatrics, Prince Sultan Military Medical City, Riyadh, Saudi Arabia.
Jehan SuleimanDivision of Neurology, Department of Pediatrics, Tawam Hospital, Al Ain, United Arab Emirates.ORCID http://orcid.org/0000-0003-0914-7650
Tawfeg Ben-OmranSidra Medicine and Research Center, Doha, Qatar.
Majid AlfadhelDepartment of Genetics and Precision Medicine, Department of Pediatrics, King Saud bin Abdulaziz University for Health Sciences, King Abdulaziz Medical City, Riyadh, Saudi Arabia.
Mohammed AlmannaiDepartment of Genetics and Precision Medicine, Department of Pediatrics, King Saud bin Abdulaziz University for Health Sciences, King Abdulaziz Medical City, Riyadh, Saudi Arabia.
Rehab AlsalehSidra Medicine and Research Center, Doha, Qatar.
Brahim TabarkiDivision of Neurology, Department of Pediatrics, Prince Sultan Military Medical City, Riyadh, Saudi Arabia.
King Saud bin Abdulaziz University for Health Sciences · SARiyadh Armed Forces Hospital · SAHamad Medical Corporation · QAKing Faisal Specialist Hospital & Research Centre · SAKing Saud University · SAUnited Arab Emirates University · AE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aromatic L-amino acid decarboxylase (AADC) deficiency is a rare inherited neurometabolic disorder that can lead to severe physical and developmental impairment. This report includes 16 patients from the Middle East and is the largest series of patients with confirmed AADC deficiency from this region reported to date. The patients displayed a range of signs and symptoms at presentation and almost all failed to reach major motor milestones. Missed and delayed diagnoses were common leading to the late introduction of targeted treatments. Eight unique variants were identified in the DDC gene, including six missense and two intronic variants. A previously undescribed variant was identified: an intronic variant between exons 13 and 14 (c.1243-10A>G). The patients were mostly treated with currently recommended medications, including dopamine agonists, vitamin B6, and monoamine oxidase inhibitors. One patient responded well, but treatment outcomes were otherwise mostly limited to mild symptomatic improvements. Five patients had died by the time of data collection, confirming that the condition is associated with premature mortality. There is an urgent need for earlier diagnosis, particularly given the potential for gene therapy as a transformative treatment for AADC deficiency when provided at an early age.  Conclusions: Delays in the diagnosis of AADC deficiency are common. There is an urgent need for earlier diagnosis, particularly given the potential for gene therapy as a transformative treatment for AADC deficiency when provided at an early age. What is Known: • Aromatic L-amino acid decarboxylase deficiency is a rare neurometabolic disorder that can lead to severe physical and developmental impairment. • Currently recommended medications provide mostly mild symptomatic improvements. What is New: • The clinical presentation of sixteen patients with confirmed AADC deficiency varied considerably and almost all failed to reach major motor milestones. • There is an urgent need for earlier diagnosis, given the potential for gene therapy as a transformative treatment for AADC deficiency when provided at an early age.

Indexed as

Amino Acid Metabolism, Inborn ErrorsAromatic-L-Amino-Acid DecarboxylasesDopamine AgonistsHumansMutationAromatic-L-Amino-Acid DecarboxylasesDDC protein, humanDopamine AgonistsAADC deficiencyCase reportDelayed diagnosisDevelopmental delayWhole exome sequencing

Identifiers

PMID36928758
PMCPMC10257624
OpenAlexW4327573026

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.