Sign Up to like & get
recommendations!
0
Published in 2022 at "Ophthalmic Genetics"
DOI: 10.1080/13816810.2022.2034168
Abstract: Tyrosinemia type II (OMIM #276600), also called RichnerHanhart Syndrome (RHS), is a rare autosomal recessive metabolic disease caused by a deficiency of the cytosolic enzyme tyrosine aminotransferase (TAT) (1). It can be detected in neonatal…
read more here.
Keywords:
tyrosinemia type;
manifestation;
pseudodendritic keratopathy;
bilateral recurrent ... See more keywords
Sign Up to like & get
recommendations!
3
Published in 2023 at "British Journal of Surgery"
DOI: 10.1093/bjs/znad080.240
Abstract: Due to the increased frequency of kidney transplantations and the high incidence of inguinal hernia in men, the coincidence of both features is not uncommon. A 58-year-old male patient with a history of a kidney…
read more here.
Keywords:
groin;
kidney;
patient;
bilateral recurrent ... See more keywords
Sign Up to like & get
recommendations!
0
Published in 2020 at "Medicine"
DOI: 10.1097/md.0000000000019079
Abstract: Abstract Introduction: Persistent Müllerian duct syndrome (PMDS) is a rare disease occurring in men with an otherwise completely normal phenotype, in which female internal sex organs are present, including a uterus, fallopian tubes, cervix, and…
read more here.
Keywords:
hernia;
recurrent inguinal;
case;
inguinal hernia ... See more keywords