Evidence map›Paper›PMID 41339098›Full record

ArticleClinical genetics2026

The Phenotypic Spectrum of Miller Syndrome: Insight From a French Cohort.

Marion Aubert Mucca, Perrine Brunelle, Martine Doco Fenzy, Clémence Vanlerberghe, Anne Dieux, Laura Feyereisen, Florence Jobic, Laurence Lode, Gwenael Le Guyader, Florence Petit and 4 more

Abstract read
In one paragraph

Article in Clinical genetics, 2026. 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
–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

1 citing paper in PubMed.

  1. 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

14 authors.

Marion Aubert MuccaService de Génétique Médicale, Hôpital Purpan, CHU Toulouse, Toulouse, France.ORCID 0000-0002-8638-2630
Perrine BrunelleInstitut de Génétique Médicale, ULR7364 RADEME, CHU Lille, Univ. Lille, Lille, France.
Martine Doco FenzyService de Génétique Médicale, CHU Reims, Reims, France.
Clémence VanlerbergheClinique de génétique « Guy Fontaine », ULR7364 RADEME, CHU Lille, Univ. Lille, Lille, France.
Anne DieuxClinique de génétique « Guy Fontaine », ULR7364 RADEME, CHU Lille, Univ. Lille, Lille, France.
Laura FeyereisenService de Génétique Médicale, CHU Reims, Reims, France.
Florence JobicService de Génétique Médicale, CHU Amiens, Amiens, France.
Laurence LodeService de Génétique Médicale, CHU Reims, Reims, France.
Gwenael Le GuyaderService de Génétique Médicale, CHU Poitiers, Poitiers, France.
Florence PetitClinique de génétique « Guy Fontaine », ULR7364 RADEME, CHU Lille, Univ. Lille, Lille, France.
Elise SchaeferService de Génétique Médicale, Institut de Génétique Médicale, hôpitaux Universitaires de Strasbourg, Strasbourg, France.
Khaoula Zaafrane-KhachnaouiService de Génétique Médicale, CHU Nice, Nice, France.
Alban ZieglerService de Génétique Médicale, Hôpital Purpan, CHU Toulouse, Toulouse, France.
Olivier PatatService de Génétique Médicale, Hôpital Purpan, CHU Toulouse, Toulouse, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Miller syndrome (MIM#263750) is a rare autosomal recessive acrofacial dysostosis associated with biallelic DHODH variants. Since the identification of the gene in 2010, five case reports have described a variable phenotype in only nine individuals from eight families. We present a cohort of 10 individuals from seven families affected by Miller syndrome, spanning the prenatal stage to 46 years of age. We report on the largest cohort of Miller syndrome to date, which highlights novel findings, including optic atrophy in multiple members of one consanguineous family. The typical postaxial limb defects, including the absence of the 5th digit, were consistent with prior descriptions, but we highlighted the frequent involvement of preaxial structures (thumb and tibial hypoplasia). A higher incidence of camptodactyly and the presence of facial nevus in two patients were notable findings. Congenital heart defects, primarily atrial septal defects, were common, and all living individuals had normal neurodevelopment. This cohort expands the phenotypic spectrum of Miller syndrome associated with variation in DHODH, presenting new findings such as preaxial involvement and facial nevus simplex. Optic atrophy in one family could prompt screening of other cases. Early prenatal diagnosis, particularly in the presence of cardinal limb and cardiac malformations, is crucial for management and genetic counseling.

Indexed as

Mandibulofacial DysostosisOxidoreductases Acting on CH-CH Group DonorsPhenotypeAdolescentAdultChildChild, PreschoolCohort StudiesFemaleFranceHumansInfantMaleMiddle AgedMutationPedigreeOxidoreductases Acting on CH-CH Group Donorsacrofacial dysostosisDHODHGenee‐Wiedemann syndromeMiller syndromeWildervanck‐Smith syndrome

Identifiers

PMID41339098
PMCPMC12674979

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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.