## Abstract A boy is described with clinical features including postβnatal short stature, short limbs, speech delay, relatively large skull, prominent metopic ridge, wide palpebral fissures, proptosis, epicanthic folds, capillary hemangioma between the eyes and nose, flat nasal bridge, everted and
β¦ LIBER β¦
A child with sclerocornea, short limbs, short stature, and distinct facial appearance
β Scribed by Thompson, Elizabeth M. ;Winter, Robin M. ;Opitz, John M. ;Reynolds, James F.
- Book ID
- 101442092
- Publisher
- John Wiley and Sons
- Year
- 1988
- Tongue
- English
- Weight
- 352 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0148-7299
No coin nor oath required. For personal study only.
β¦ Synopsis
We describe a boy with sclerocornea, short limbs, short stature and a distinct facial appearance. The resemblance to other reports of affected sibs suggests
π SIMILAR VOLUMES
Post-natal short stature, short limbs, b
β
AndrΓ© MΓ©garbanΓ©; Simon Rassi; Farid Estephan; Edith Kouba-Hreich
π
Article
π
2003
π
John Wiley and Sons
π
English
β 139 KB
π 1 views
A new syndrome short limbs, abnormal fac
β
Barrow, M. ;Fitzsimmons, J. S. ;Fraser, F. C. ;Prevs, M.
π
Article
π
1984
π
John Wiley and Sons
π
English
β 186 KB
Developmental delay, short stature, and
β
Chodirker, Bernard N. ;Ray, Manoranjan ;McAlpine, Phyllis J. ;Riordan, Diane ;Vu
π
Article
π
1988
π
John Wiley and Sons
π
English
β 419 KB
π 2 views
Mental retardation with pterygia, shortn
β
M. Haspeslagh; J. P. Fryns; A. de MΓ»elenaere; L. Schautteet; I. van Eeckhoutte;
π
Article
π
2008
π
John Wiley and Sons
π
English
β 464 KB
Four siblings with distal renal tubular
β
Eissa Faqeih; Samhar I. Al-Akash; Nadia Sakati; Prof. Ahmad S. Teebi
π
Article
π
2007
π
John Wiley and Sons
π
English
β 329 KB
π 2 views
Short stature, myopia, severe developmen
β
Achermann, Sibylla; Largo, Remo; Kotzot, Dieter; Riegel, Mariluce; Schinzel, Alb
π
Article
π
1999
π
John Wiley and Sons
π
English
β 44 KB
π 2 views
We report on 2 brothers with short stature, microcephaly, myopia, retarded osseous maturation, severe developmental delay, and minor anomalies including temporal narrowing, periorbital fullness, full cheeks in infancy, and protruding lower lip. Both brothers and their parents had normal chromosomes.