We report on a female with lymphedema, facial anomalies, intestinal lymphangiectasia, and moderate mental retardation consistent with the diagnosis of Hennekam syndrome. In addition, she had a number of other anomalies not previously described in this autosomal recessive disorder, including a congen
β¦ LIBER β¦
Craniosynostosis and kidney malformation in a case of Hennekam syndrome
β Scribed by Cormier-Daire, V. ;Lyonnet, S. ;Lehnert, A. ;Martin, D. ;Salomon, R. ;Patey, N. ;Broyer, M. ;Ricour, C. ;Munnich, A.
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- English
- Weight
- 409 KB
- Volume
- 57
- Category
- Article
- ISSN
- 0148-7299
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
Expansion of the phenotype in Hennekam s
β
Angle, Brad; Hersh, Joseph H.
π
Article
π
1997
π
John Wiley and Sons
π
English
β 22 KB
π 2 views
Baller-Gerold syndrome: An 11th case of
β
Boudreaux, Jeanne M. ;Colon, Marc A. ;Lorusso, Giovanni D. ;Parro, Elizabeth A.
π
Article
π
1990
π
John Wiley and Sons
π
English
β 421 KB
π 2 views
We report on a patient with craniosynostosis, left radius aplasia, right radius hypoplasia, and other congenital anomalies. This is the 11th reported case of the Baller-Gerold syndrome. Autosomal recessive inheritance of this syndrome is suggested by evidence of probable parental consanguinity.
A sixth report (eighth case) of craniosy
β
Pelias, Mary Z. ;Superneau, Duane W. ;Thurmon, Theodore F. ;Opitz, John M.
π
Article
π
1981
π
John Wiley and Sons
π
English
β 393 KB
π 2 views
Severe lymphedema, intestinal lymphangie
β
Forzano, F. ;Faravelli, F. ;Loy, A. ;Di Rocco, M.
π
Article
π
2002
π
John Wiley and Sons
π
English
β 116 KB
π 2 views
Spontaneous disappearance of lung metast
β
M. F. Nicholls; A. H. M. Siddons
π
Article
π
1960
π
John Wiley and Sons
π
English
β 321 KB
Hypothelia, syndactyly, and ear malforma
β
Hagit Baris; Wen-Hann Tan; Virginia E. Kimonis
π
Article
π
2005
π
John Wiley and Sons
π
English
β 107 KB
π 1 views