Blepharophimosis
Human disease
Blepharophimosis is a congenital anomaly in which the eyelids are underdeveloped such that they cannot open as far as usual and permanently cover part of the eyes. The horizontal palpebral fissure (eyelid opening) is shortened; the eyes also appear spaced more widely apart as a result, known as telecanthus.
Nº Q883850 ★
Común · Saberes
Blepharophimosis
Human disease
Blepharophimosis is a congenital anomaly in which the eyelids are underdeveloped such that they cannot open as far as usual and permanently cover part of the eyes. The horizontal palpebral fissure (eyelid opening) is shortened; the eyes also appear spaced more widely apart as a result, known as telecanthus.
Último precio
—
Precio mínimo
—
Mediana 7 d
—
Ventas 30 d
0
Rango 30 d
—
En circulación
0
Cotización
mediana
mín – máx
ventas
Sin ventas en el periodo
Ver tabla
| Fecha | mediana | Mín | Máx | ventas |
|---|
Historial de ventas
- Última venta
- —
- Media 30 d
- —
- Mínimo 30 d
- —
- Máximo 30 d
- —
- Ventas 7 d
- 0
- Ventas 30 d
- 0
Aún no hay ventas.
Ventas anónimas: sin comprador ni vendedor. Las cifras solo cuentan ventas entre jugadores.
En Wikipedia
Texto en inglés Aún no hay artículo en tu idioma: extracto en inglés.
Blepharophimosis is a congenital anomaly in which the eyelids are underdeveloped such that they cannot open as far as usual and permanently cover part of the eyes. The horizontal palpebral fissure (eyelid opening) is shortened; the eyes also appear spaced more widely apart as a result, known as telecanthus.
Texto: Wikipedia en inglés, CC BY-SA 4.0. · Imagen: Grzechocińska, B., Warzecha, D., Wypchło, M. et al. (CC BY 4.0) ·
Cartas cercanas
Ptosis palpebral
Descenso permanente del párpado superior
Nº Q622427 ★★★
Blepharochalasis
Eyelid disease that is characterized by exacerbations and remissions of eyelid edema, which results in a stretching and subsequent atrophy of the eyelid tissue, leading to the formation of redundant folds over the lid margins
Nº Q3640920 ★★
Erythropoietic protoporphyria
Acute porphyria characterized by a deficiency in the enzyme ferrochelatase, leading to abnormally high levels of protoporphyrin in the tissue
Nº Q1759600 ★★
Síndrome de encefalopatía posterior reversible
Nº Q7234232 ★★
Síndrome de Bloom
Nº Q1469646 ★★
Fisura palpebral
Nº Q7128693 ★