Bannayan-Zonana syndrome is a rare entity characterized by macro-\ud cephaly and multiple soft tissue and visceral hamartomas and\ud lipomas. Knowledge of this syndrome is important given the risk\ud of sometimes fatal bleeding and visceral neoplasia in adulthood. We\ud report on a new case, original in its sporadic occurrence and rapidly\ud fatal progression
Cowden syndrome (OMIM No. 158350) and Bannayan-Riley-Ruvalcaba syndrome (BRRS) (OMIM No. 153480) are...
Bannayan-Rıley-Ruvalcaba syndrome (BRRS) is characterized by macrocephaly, pigmented macules on the ...
BACKGROUND: Phosphatase and tensin homolog (PTEN) hamartoma tumor syndrome (PHTS) encompasses sever...
Bannayan-Rilay-Ruvalcaba syndrome (BRRS) is a rare congenital disorder, characterized by macrocephal...
Bannayan–Riley–Ruvalcaba syndrome (BRRS, [OMIM 153480]) is characterized by macrocephaly, lipomatosi...
Bannayan-Riley-Ruvalcaba syndrome (BRRS) is a rare autosomal, dominantly-inherited, hamartoma syndro...
Cowden syndrome (OMIM No 158350) is a pleomorphic, autosomal dominant syndrome characterised by hama...
A síndrome de Cowden (SC) ou síndrome de múltiplos hamartomas (SMH) é genodermatose rara de herança ...
Bannayan-Riley-Ruvalcaba syndrome (BRRS) is a rare autosomal, dominantly-inherited, hamartoma syndro...
Cowden's disease or multiple hamartoma syndrome is an autosomal dominant inherited disease and the m...
Bannayan-Riley-Ruvalcaba Syndrome is a rare condition caused by mutations in the PTEN gene. It displ...
ERKEK, BULENT/0000-0002-9041-341X; ULKATAN, SEDAT/0000-0002-9288-7635WOS: 000232067800012PubMed: 161...
The B.N.S. shows certain similarities to other systemic diseases. these diseases are often referred ...
Brunner’s gland hamartomas are rare tumours of the duo-denum. These lesions have previously been des...
Bannayan-Riley-Ruvalcaba syndrome (BRRS) is characterised by macrocephaly, intestinal hamartomatous ...
Cowden syndrome (OMIM No. 158350) and Bannayan-Riley-Ruvalcaba syndrome (BRRS) (OMIM No. 153480) are...
Bannayan-Rıley-Ruvalcaba syndrome (BRRS) is characterized by macrocephaly, pigmented macules on the ...
BACKGROUND: Phosphatase and tensin homolog (PTEN) hamartoma tumor syndrome (PHTS) encompasses sever...
Bannayan-Rilay-Ruvalcaba syndrome (BRRS) is a rare congenital disorder, characterized by macrocephal...
Bannayan–Riley–Ruvalcaba syndrome (BRRS, [OMIM 153480]) is characterized by macrocephaly, lipomatosi...
Bannayan-Riley-Ruvalcaba syndrome (BRRS) is a rare autosomal, dominantly-inherited, hamartoma syndro...
Cowden syndrome (OMIM No 158350) is a pleomorphic, autosomal dominant syndrome characterised by hama...
A síndrome de Cowden (SC) ou síndrome de múltiplos hamartomas (SMH) é genodermatose rara de herança ...
Bannayan-Riley-Ruvalcaba syndrome (BRRS) is a rare autosomal, dominantly-inherited, hamartoma syndro...
Cowden's disease or multiple hamartoma syndrome is an autosomal dominant inherited disease and the m...
Bannayan-Riley-Ruvalcaba Syndrome is a rare condition caused by mutations in the PTEN gene. It displ...
ERKEK, BULENT/0000-0002-9041-341X; ULKATAN, SEDAT/0000-0002-9288-7635WOS: 000232067800012PubMed: 161...
The B.N.S. shows certain similarities to other systemic diseases. these diseases are often referred ...
Brunner’s gland hamartomas are rare tumours of the duo-denum. These lesions have previously been des...
Bannayan-Riley-Ruvalcaba syndrome (BRRS) is characterised by macrocephaly, intestinal hamartomatous ...
Cowden syndrome (OMIM No. 158350) and Bannayan-Riley-Ruvalcaba syndrome (BRRS) (OMIM No. 153480) are...
Bannayan-Rıley-Ruvalcaba syndrome (BRRS) is characterized by macrocephaly, pigmented macules on the ...
BACKGROUND: Phosphatase and tensin homolog (PTEN) hamartoma tumor syndrome (PHTS) encompasses sever...