Anophthalmia-plus syndrome with unusual findings. A clinical report and review of the literature.
Genet Couns
; 24(3): 307-12, 2013.
Article
em En
| MEDLINE
| ID: mdl-24341146
We present a male child at 3 years old with Anophthalmia-Plus Syndrome (APS). He has asymmetry of the face and head, left choanal atresia, a sunken facial appearance, microphthalmia in the right eye, severe microphthalmia in the left eye, bilateral low-set ears, scarring from cleft palate surgery. Magnetic resonance imaging (MRI) sections revealed decreased right globe volume, an undeveloped left globe, decreased left optical nerve thickness, Chiari type 2 malformation, left choanal atresia and cleft palate. Echocardiography and abdominal ultrasonography were normal. The patient has a 45 dB conductive hearing loss in the left ear. Repeated thyroid function tests were evaluated as compatible with central hypothyroidism. We report a Fryns Anophthalmia-Plus Syndrome in a child with unusual findings including central hypothyroidism, chiari type 2 malformation, conductive hearing loss and developmental regression. Summary of the features reported in the present case and all 14 previous cases that might be defined as APS.
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Base de dados:
MEDLINE
Assunto principal:
Malformação de Arnold-Chiari
/
Anormalidades Múltiplas
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Deficiências do Desenvolvimento
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Anoftalmia
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Perda Auditiva Condutiva
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Hipotireoidismo
Idioma:
En
Ano de publicação:
2013
Tipo de documento:
Article