[National protocol for diagnosis and care of congenital aniridia: Summary for the attending physician].

Protocole national de diagnostic et de soins (PNDS) de l’aniridie congénitale : synthèse pour le médecin traitant.
Aniridie congénitale Cataract Cataracte Congenital aniridia Foveal hypoplasia Gillespie syndrome Glaucoma Glaucome Gène PAX6 Handicap visuel Hypoplasie fovéolaire PAX6 gene Syndrome WAGR Syndrome de Gillespie Visual impairment WAGR syndrome

Journal

Journal francais d'ophtalmologie
ISSN: 1773-0597
Titre abrégé: J Fr Ophtalmol
Pays: France
ID NLM: 7804128

Informations de publication

Date de publication:
Jun 2022
Historique:
received: 28 12 2021
accepted: 10 01 2022
entrez: 6 6 2022
pubmed: 7 6 2022
medline: 9 6 2022
Statut: ppublish

Résumé

Congenital aniridia is a rare panocular disease defined by a national diagnostic and care protocol (PNDS) validated by the HAS. In most cases, it is due to an abnormality in the PAX6 gene, located at 11p13. Aniridia is a potentially blinding autosomal dominant disease with high penetrance. The prevalence varies from 1/40,000 births to 1/96,000 births. Approximately one third of cases are sporadic. Ocular involvement includes complete or partial absence of iris tissue, corneal opacification with neovascularization, glaucoma, cataract, foveal hypoplasia, optic disc hypoplasia and ptosis. These ocular disorders coexist to varying degrees and progress with age. Congenital aniridia manifests in the first months of life as nystagmus, visual impairment and photophobia. A syndromic form such as WAGR syndrome, WAGRO syndrome (due to the risk of renal Wilms tumor) or Gillespie syndrome (cerebellar ataxia) must be ruled out. Systemic associations may include diabetes, due to expression of the PAX6 gene in the pancreas, as well as other extraocular manifestations. Initial assessment is best carried out in a referral center specialized in rare ophthalmologic diseases, with annual follow-up. The management of progressive ocular involvement must be both proactive and responsive, with medical and surgical management. Visual impairment and photophobia result in disability, leading to difficulties in mobility, movement, communication, learning, fine motor skills, and autonomy, with consequences in personal, school, professional, socio-cultural and athletic life. Medico-socio-educational care involves a multidisciplinary team. Disability rehabilitation must be implemented to prevent and limit situations of handicap in activities of daily living, relying on the Commission for the Rights and Autonomy of People with Disabilities (CDAPH) within the Departmental House of People with Disabilities (MDPH). The general practitioner coordinates multidisciplinary medical and paramedical care.

Identifiants

pubmed: 35667788
pii: S0181-5512(22)00133-4
doi: 10.1016/j.jfo.2022.01.005
pii:
doi:

Types de publication

Journal Article Review

Langues

fre

Sous-ensembles de citation

IM

Pagination

647-652

Investigateurs

Dominique Bremond-Gignac (D)
Vincent Borderie (V)
Jean-Louis Bourges (JL)
Patrick Calvas (P)
Frédéric Chiambaretta (F)
Henri Copin (H)
Vincent Daien (V)
Antoine Labbé (A)
Béatrice Le Bail (B)
Bruno Mortemousque (B)
Matthieu Robert (M)
Jean-Michel Rozet (JM)
Arnaud Sauer (A)
Sophie Valleix (S)
Daniel Aberdam (D)
Marc Abitbol (M)
Nathalie Aidan (N)
Isabelle Audo (I)
Nadia Bahi-Buisson (N)
Emmanuelle Barbieri (E)
Fernand Basille (F)
Aurélie Bouet (A)
Lénaïc Bruere (L)
Joseph Bursztyn (J)
Béatrice Cochener-Lamard (B)
Alejandra Daruich-Matet (A)
Danièle Denis (D)
Philippe Denis (P)
Nathalie De Vergnes (N)
Adil El Maftouhi (A)
Audrey Forbeaux Glize (A)
Eric Gabison (E)
Jean Philippe Grundeler (JP)
Louis Hoffart (L)
Sophie Igla (S)
Gaëlle Jouanjan (G)
Elsa Laumonier Demory (E)
Camille Leroy (C)
Guylène Le Meur (G)
Zoia Mincheva (Z)
Elisabeth Plat (E)
Charlotte Rigal-Sastourne (C)
Serge Romana (S)
Antoine Rousseau (A)
Rémi Salomon (R)
Julie Steffann (J)
Valérie Touitou (V)
Alain Verloes (A)

Informations de copyright

Copyright © 2022 Elsevier Masson SAS. All rights reserved.

Auteurs

D Bremond-Gignac (D)

Service d'ophtalmologie, centre hospitalier universitaire Necker-Enfants Malades, AP-HP, université de Paris, 149, rue de Sèvres, 75015 Paris, France; Inserm 1138, T17, université de Paris, Paris, France; OPHTARA, Coordonnateur centre de maladies rares en ophtalmologie (CRMR), Filière Sensgene, centre hospitalier universitaire Necker-Enfants Malades, Paris, France. Electronic address: dominique.bremond@aphp.fr.

M Robert (M)

Service d'ophtalmologie, centre hospitalier universitaire Necker-Enfants Malades, AP-HP, université de Paris, 149, rue de Sèvres, 75015 Paris, France; OPHTARA, Coordonnateur centre de maladies rares en ophtalmologie (CRMR), Filière Sensgene, centre hospitalier universitaire Necker-Enfants Malades, Paris, France.

A Daruich (A)

Service d'ophtalmologie, centre hospitalier universitaire Necker-Enfants Malades, AP-HP, université de Paris, 149, rue de Sèvres, 75015 Paris, France; Inserm 1138, T17, université de Paris, Paris, France; OPHTARA, Coordonnateur centre de maladies rares en ophtalmologie (CRMR), Filière Sensgene, centre hospitalier universitaire Necker-Enfants Malades, Paris, France.

V Borderie (V)

Ophtalmologie, CHNO des XV-XX, Paris, France.

F Chiambaretta (F)

Ophtalmologie, CHU de Clermont-Ferrand, Clermont-Ferrand, France.

S Valleix (S)

Inserm 1138, T17, université de Paris, Paris, France; Laboratoire de génétique moléculaire, centre hospitalier universitaire Necker-Enfants Malades, AP-HP, université de Paris, Paris, France.

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