These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


PUBMED FOR HANDHELDS

Search MEDLINE/PubMed


  • Title: [Familial syndrome of microcephaly with oculocutaneous albinism and digital anomalies].
    Author: Castro-Gago M, Pombo M, Novo I, Tojo R, Peña J.
    Journal: An Esp Pediatr; 1983 Aug; 19(2):128-31. PubMed ID: 6660641.
    Abstract:
    Authors make a report concerning a male patient who presents microcephaly, oculocutaneus albinism, hypoplasia of the distal phalanx of the 1st, 3rd and 4th finger of the right hand, 1st, 3rd, 4th and 5th finger of the left hand and agenesia of the distal end of the big toe of the right foot. They think it is a new dysmorphic syndrome. Because of patient's sister presented a similar picture they suggest that it may be an autosomal recessive inheritance pattern.
    [Abstract] [Full Text] [Related] [New Search]