Total: 1 |
|
PMID (PMCID) | ||
---|---|---|
16152639 |
MIXED_SAMPLE | Child |
Autosomal recessive Oliver-McFarlane syndrome: retinitis pigmentosa, short stature (GH deficiency), trichomegaly, and hair anomalies or CPD syndrome (chorioretinopathy-pituitary dysfunction). | ||
Haimi M, Gershoni-Baruch R. Am J Med Genet A. 2005;138A(3):268-71. |
||
We describe a brother and sister with retinitis pigmentosa (RP), growth failure, long eyelashes, and sparse hair. |