Clean and clear (out): A neat method for the recovery of latent fingermarks from crime-scenes.

Crime-scenes are the heart of any investigation in terms of recovery of key forensic evidence - fingermarks and DNA. Yet, quite often, the operational work of the forensic units, in which different chemicals and reagents for fingermarks development are applied, can also be highly destructive to the property and the environment. Hence, for both ecological and intelligence purposes, an operational method that minimizes that damage would be ideal. In this study, an "out-of-the-box" approach is proposed; rather than working at the crime scene itself, gel-lifters were used as a transferring tool for the latent forensic evidence, fingermarks and DNA, to be developed by applying black wet-powder (Wetwop®) in a controlled laboratory environment, leaving the crime-scene undisturbed. The results show a promising potential, as this indirect method proved to be robust and successful for non-porous surfaces, and even for aged fingermarks. In addition, this study gave a new perspective into the accepted notion regarding the difference between male and female donors, showing a direct correlation of the size and weight of the hands to the natural pressure applied by the donor. Moreover, the indirect nature of the method highlights the importance of the interaction between the type of surface and the latent fingermark constituents, primarily water, and its effect on the survivability and quality of the developed fingermark. Due to the growing demand of keeping crime scenes and exhibits unharmed by both police and intelligence forces, the new approach of this application provides a valuable asset for future operational field-work.

What is the best treatment for women with polycystic ovarian syndrome and high LH/FSH ratio? A comparison among in vitro fertilization with GnRH agonist, GnRH antagonist and in vitro maturation.

PURPOSE: To evaluate whether high LH/FSH ratio has a clinical impact on patients with polycystic ovary syndrome (PCOS) undergoing in vitro fertilization (IVF) with GnRH-agonist/antagonist protocols or in vitro maturation (IVM) treatments. METHODS: We retrospectively reviewed all PCOS patients with day 3 LH/FSH ratio ≥1.5 who underwent IVF or IVM. The main outcomes measures were embryo quality and pregnancy rate. RESULTS: A total of 75 cycles were included. Among these, 44 patients underwent long agonist protocol, 16 antagonist protocol and 15 IVM. Age, basal LH and FSH levels, as well as duration of infertility were comparable for all groups. The LH level on the day of hCG administration was significantly lower in the antagonist group (0.9 IU/ml) compared to the long agonist group (1.4 IU/ml, p = 0.01). There was no difference in pregnancy rates among the groups: 27.2 % in the long agonist group, 37.5 % in the antagonist group and 26.6 % among the IVM patients. CONCLUSIONS: High LH/FSH ratio had no adverse effect on pregnancy rates in all three treatment modes.

Non-syndromic autosomal recessive congenital ichthyosis in the Israeli population.

BACKGROUND: Autosomal recessive congenital ichthyosis (ARCI) is the term given to a complex and heterogeneous group of cornification disorders associated with mutations in at least eight distinct genes. Mutation distribution and prevalence rates are instrumental for the design of diagnostic strategies in ARCI but have not yet been systematically explored in the Israeli population. Previous data suggest that the demographic features specific to Middle Eastern populations, such as a high frequency of consanguineous marriages, may have an effect on the molecular epidemiology of genodermatoses. METHODS: We systematically assessed all families with ARCI presenting at our clinics over a period of 9 years, using a combination of homozygosity mapping, direct sequencing and PCR-restriction fragment length polymorphism assays. RESULTS: In total, 20 families with ARCI were assessed, and causative mutations were identified in 7 genes: TGM1 (30% of patients), ALOX12B (20%), ABCA12 (5%), CYP4F22 (10%), ALOXE3 (10%), LIPN (5%) and NIPAL4 (5%) Two families (10%) had mutations mapped to an ARCI-associated locus on 12p11.2-q13, while no mutation was found for one additional kindred. In the subgroup of families of Arab Muslim origin, mutations were identified most frequently in ALOX12B and TGM1 (31%), whereas the other subgroups displayed a subtype distribution very similar to that previously reported in western populations. CONCLUSIONS: The present data point to the need for population-tailored mutation screening strategies in genetically heterogeneous genodermatoses, based on the relative prevalence of the disease subsets.