Cargando…
Familial clustering of a rare syndrome
Ectrodactyly, ectodermal dysplasia and cleft palate syndrome is a rare autosomal dominant multiple congenital anomaly syndrome with variable expressivity and reduced penetration. The cardinal features are cleft palate/lip, lobster hand deformity, sparse hypopigmented hair, dry scaly skin, and lacrim...
Autores principales: | Nadkarni, Jayashree, Ganesh, Hari, Dwivedi, Rashmi |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3144684/ https://www.ncbi.nlm.nih.gov/pubmed/21814340 http://dx.doi.org/10.4103/0971-6866.82189 |
Ejemplares similares
-
Quality of life in children with epilepsy
por: Nadkarni, Jayashree, et al.
Publicado: (2011) -
Brooke–Spiegler Syndrome: Familial Cylindromatosis, a Rare Variant of a Rare Familial Syndrome
por: Patel, Harsh, et al.
Publicado: (2021) -
Purtscher-like retinopathy: A rare ocular finding in nephrotic syndrome
por: Dwivedi, Anamika, et al.
Publicado: (2018) -
Harlequin Syndrome in a Case of Toxic Goitre: A Rare Association
por: Pradeep, P. V., et al.
Publicado: (2011) -
Warkany Syndrome: A Rare Case Report
por: Agrawal, Amit, et al.
Publicado: (2011)