Robinow syndrome

Journal of Postgraduate Medicine

Volumn 48, Issue 1, 2002, Pages 50-51

  Hosalkar, H S ^a   Gerardi, J ^b   Shaw, B A ^b  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

ANTHROPOMETRY; ARTICLE; B LYMPHOCYTE; BIRTH DEFECT; BODY HEIGHT; BONE AGE; BONE RADIOGRAPHY; BRACHYDACTYLY; CAMPTODACTYLY; CASE REPORT; COMPUTER ASSISTED TOMOGRAPHY; CORPUS CALLOSUM AGENESIS; DEVELOPMENTAL DISORDER; FACE DYSMORPHIA; FAMILY HISTORY; FEMALE; GENITAL MALFORMATION; HEAD CIRCUMFERENCE; HORMONE DETERMINATION; HUMAN; INTELLIGENCE QUOTIENT; LYMPHOCYTE FUNCTION; MEDICAL EXAMINATION; NEWBORN JAUNDICE; RESPIRATORY TRACT INFECTION; ROBINOW SYNDROME; SCHOOL CHILD; SCOLIOSIS; SEXUAL MATURITY; SHORT STATURE; T LYMPHOCYTE;

ABNORMALITIES, MULTIPLE; CHILD; DWARFISM; FACE; FEMALE; HUMANS; HYPOGONADISM; SYNDROME;

EID: 0036064330     PISSN: 00223859     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (10)

1. A newly recognized dwarfing syndrome
2. Robinow syndrome
3. Robinow syndrome: Report of one case
4. The Robinow (fetal face) syndrome: A continuing puzzle
5. Mutation of the gene encoding the ROR2 tyrosine kinase causes autosomal recessive Robinow syndrome
6. Recessive Robinow syndrome, allelic to dominant brachydactyly type B, is caused by mutation of ROR2
7. Robinow's syndrome. Partial primary hypogonadism in pubertal boys, with persistence of micropenis
8. Robinow syndrome: Prenatal diagnosis
9. Robinow syndrome with growth hormone deficiency: Treatment with growth hormone
10. Recessive Robinow syndrome: With emphasis on endocrine functions