Cancers, Vol. 16, Pages 1420: Growth Charts for Shwachman & ndash;Diamond Syndrome at Ages 0 to 18 Years
Cancers, Vol. 16, Pages 1420: Growth Charts for Shwachman–Diamond Syndrome at Ages 0 to 18 Years
Cancers doi: 10.3390/cancers16071420
Authors:
Anna Pegoraro
Valentino Bezzerri
Gloria Tridello
Cecilia Brignole
Francesca Lucca
Emily Pintani
Cesare Danesino
Simone Cesaro
Francesca Fioredda
Marco Cipolli
Shwachman–Diamond syndrome (SDS) is one of the most common inherited bone marrow failure syndromes. SDS is characterized by hypocellular bone marrow, with a severe impairment of the myeloid lineage, resulting in neutropenia, thrombocytopenia, and, more rarely, anemia. Almost 15...
Source: Cancers - April 5, 2024 Category: Cancer & Oncology Authors: Anna Pegoraro Valentino Bezzerri Gloria Tridello Cecilia Brignole Francesca Lucca Emily Pintani Cesare Danesino Simone Cesaro Francesca Fioredda Marco Cipolli Tags: Communication Source Type: research
Update on cancer predisposition syndromes and surveillance guidelines for childhood brain tumors
Clin Cancer Res. 2024 Apr 4. doi: 10.1158/1078-0432.CCR-23-4033. Online ahead of print.ABSTRACTTumors of the central nervous system (CNS) comprise the second most common group of neoplasms in childhood. The incidence of germline predisposition among children with brain tumors continues to grow as our knowledge on disease aetiology increases. Some children with brain tumors may present with non-malignant phenotypic features of specific syndromes (e.g. nevoid basal cell carcinoma syndrome, neurofibromatosis type 1 and type 2, DICER1 syndrome, and constitutional mismatch repair deficiency), while others may present with a str...
Source: Cell Research - April 4, 2024 Category: Cytology Authors: Jordan R Hansford Anirban Das Rose B McGee Yoshiko Nakano Jack Brzezinski Sarah R Scollon Surya P Rednam Jaclyn Schienda Orli Michaeli Sun Young Kim Mary-Louise C Greer Rosanna Weksberg Douglas R Stewart William D Foulkes Uri Tabori Kristian W Pajtler Ste Source Type: research
Update on cancer predisposition syndromes and surveillance guidelines for childhood brain tumors
Clin Cancer Res. 2024 Apr 4. doi: 10.1158/1078-0432.CCR-23-4033. Online ahead of print.ABSTRACTTumors of the central nervous system (CNS) comprise the second most common group of neoplasms in childhood. The incidence of germline predisposition among children with brain tumors continues to grow as our knowledge on disease aetiology increases. Some children with brain tumors may present with non-malignant phenotypic features of specific syndromes (e.g. nevoid basal cell carcinoma syndrome, neurofibromatosis type 1 and type 2, DICER1 syndrome, and constitutional mismatch repair deficiency), while others may present with a str...
Source: Clinical Cancer Research - April 4, 2024 Category: Cancer & Oncology Authors: Jordan R Hansford Anirban Das Rose B McGee Yoshiko Nakano Jack Brzezinski Sarah R Scollon Surya P Rednam Jaclyn Schienda Orli Michaeli Sun Young Kim Mary-Louise C Greer Rosanna Weksberg Douglas R Stewart William D Foulkes Uri Tabori Kristian W Pajtler Ste Source Type: research
Update on cancer predisposition syndromes and surveillance guidelines for childhood brain tumors
Clin Cancer Res. 2024 Apr 4. doi: 10.1158/1078-0432.CCR-23-4033. Online ahead of print.ABSTRACTTumors of the central nervous system (CNS) comprise the second most common group of neoplasms in childhood. The incidence of germline predisposition among children with brain tumors continues to grow as our knowledge on disease aetiology increases. Some children with brain tumors may present with non-malignant phenotypic features of specific syndromes (e.g. nevoid basal cell carcinoma syndrome, neurofibromatosis type 1 and type 2, DICER1 syndrome, and constitutional mismatch repair deficiency), while others may present with a str...
Source: Clinical Cancer Research - April 4, 2024 Category: Cancer & Oncology Authors: Jordan R Hansford Anirban Das Rose B McGee Yoshiko Nakano Jack Brzezinski Sarah R Scollon Surya P Rednam Jaclyn Schienda Orli Michaeli Sun Young Kim Mary-Louise C Greer Rosanna Weksberg Douglas R Stewart William D Foulkes Uri Tabori Kristian W Pajtler Ste Source Type: research
A Novel TSHR Gene Mutation in a Family with Non-autoimmune Hyperthyroidism
CONCLUSIONS: This novel TSHR variant is associated with T3 toxicosis during childhood. Therefore, early identification and treatment may improve patient outcomes.PMID:38566871 | PMC:PMC10983094 | DOI:10.5455/medarh.2024.78.154-158 (Source: Cancer Control)
Source: Cancer Control - April 3, 2024 Category: Cancer & Oncology Authors: Tamara Kufoof Catherine Luxford Kishani Kannangara Roderick Clifton-Bligh Kim C Donaghue Source Type: research
Cancer patterns in Arua district, Uganda: a hospital-based retrospective study
CONCLUSION: There is a high incidence of liver cancer in Arua district. The high levels of cervical, breast and oesophagus cancer were consistent with what is reported by the two PBCRs in Uganda. However, BL could be due to the presence of a BL treatment centre at Kuluva hospital in Arua. Cancer interventions in Arua should therefore be targeted towards liver, cervix, breast, and oesophagus cancer and furthering research on the reason for the high incidence of liver cancer.PMID:38566768 | PMC:PMC10984836 | DOI:10.3332/ecancer.2024.1688 (Source: Ecancermedicalscience)
Source: Ecancermedicalscience - April 3, 2024 Category: Cancer & Oncology Authors: Bridget Angucia Sharon Annet Nakaganda Geriga Fadhil Micah June Ezra Anecho Gilbert Aniku Amandua Jacinto Hesborn Wao Jackson Orem Onguru Daniel Source Type: research
