"In my view the approach of the family court to earlier findings has three stages: firstly, the court considers whether it will permit any reconsideration or review of or challenge to the earlier finding, here referred to by the parents as a review. If it does, the second and third stages relate to its approach to that exercise. The second stage relates to and determines the extent of the investigations and evidence concerning the review. The third stage is the hearing of the review, and thus it is at this stage that the court decides the extent to which the earlier findings stand, by applying the relevant test of the circumstances then found to exist."
"The same three-stage approach applies in my judgment whether the issue arises before the same judge or a different judge; whether in the same or different proceedings; and whether in relation to the same or different children. I do not, with all respect to Baker J's tentative comments, think that different approaches are called for in different forensic contexts. The attempt to create such a forensic taxonomy would, I fear, be productive merely of satellite litigation. Of course the application of the general approach in any particular case will reflect the circumstances of that case. "
"Above all, the court is bound to want to consider whether there is any reason to think that a rehearing of the issue will result in any different finding from that in the earlier trial. By this I mean something more than the mere fact that different judges might on occasions reach different conclusions upon the same evidence. The court will want to know whether there is any new evidence or information casting doubt upon the accuracy of the original findings."
"I do not understand the President to be equating the test at 'stage 1' ("some real reason to believe the earlier findings require revisiting" of Re ZZ) with the test which is to be applied on an application for permission to appeal. That is to say, I do not have to satisfy myself that the mother stands a 'real prospect of success' of disturbing the original findings, or that there is 'some other compelling reason' why the case should be heard. The test in these circumstances is not so exacting. "
"I would emphasise that in my opinion, and I also think that of the other experts, is there have been two separate episodes of bony injury. The rib fracture happened probably several weeks before the knee and elbow injuries, which may have occurred at the same time. Both these events are more likely that not to be inflicted non-accidental injuries based on the type of injuries seen, and the lack of any plausible explanation. "
"Fractures to the metaphysis are highly specific for non-accidental injury, hence the term 'classic metaphyseal lesions' that is often applied. The mechanism for the injury is a torsional twisting force combined with a distraction pulling force. However, studies on infant pigs suggest the distraction force may be more important than the torsional force. Accidental rib fractures in infants and young children are extremely rare. They only occur in sever traumatic episodes, such as unrestrained child in a motor vehicle accident, or a crushing injury; and in such circumstances are associated with mortality rates of 40 to 50 per cent. Rib fractures may occur in children with metabolic or inherited bone disorders, for example, osteogenesis imperfecta. There is no evidence for that here."
"E is vitamin D insufficient. The test result is 25.8 Nano molecules per litre. The parents' levels are also insufficient. None are deficient in vitamin D. Vitamin D insufficiency, deficiency, may be caused by insufficient dietary intake, and low exposure to sunlight. In utero, the foetus obtains vitamin D from the mother via the placenta, and is therefore dependent on mother's vitamin D levels. Breast milk contains little vitamin D, and therefore a vitamin D deficient mother may not provide sufficient vitamin D in her breast milk to prevent insufficiency, deficiency in the infant. Formula milk is fortified with vitamin D, and therefore bottle-fed children are rarely vitamin D deficient. "
"Osteogenesis imperfecta type 1 is characterised chiefly by multiple bone fractures, usually resulting from minimal trauma. Affected individuals have blue sclerae, normal teeth, and normal or near-normal stature. Fractures are rare in the neonatal period, up to the age of one month. Fracture tendency is constant from childhood to puberty, decreases thereafter, and often increases following menopause in women, and after the sixth decade in men. Fractures heal rapidly with evidence of good callous formation, and with good orthopaedic care, without deformity. "
"The determination of bone density on x-rays is a subjective and qualitative assessment. With high quality radiographs, the assessment that bone density is normal is usually straightforward. However, the assessment of reduced bone density is more difficult. In adults it is believed that approximately 40 per cent of bone mineralisation needs to be lost before it becomes obvious on x-ray. There is no comparable data in children. In addition, poor quality x-rays or variations in technique and/or post-processing of digital x-rays can lead to a false assessment of reduced bone density. "
"I confirm that at the hearing on 7 May, I confirmed that I accepted there are no other medical explanations for E's fractures. I came to this view after going back over all of the medical evidence. On the medical evidence which is available to me, I do accept that the injuries are non-accidental injuries. I cannot explain how the injuries occurred, or when they occurred, but I do know that I have not knowingly injured E in the normal course of caring for her. I do however accept that I do now have to draw a line under the medical evidence, and I am not seeking any further medical assessment or tests on E regarding the court's findings. "
"We have recently been in contact with Rachel Carter from Wollen Michelmore, who highly recommended yourself. We were wondering if you could view two sets of x-rays that we have, as there are inconsistencies between them. The first set of x-rays were done at Northampton General in April 2012 when E was 7 weeks' old. The second set was done at Great Ormond Street Hospital in October 2012 when E was 8 months' old. Also, when she was at Great Ormond Street, blue sclerae was seen, and mild diminished bone density was reported. We had vitamin D testing done in August 2012. My result was 26.8, my husband was 26.9, and our daughter was 25.8. At this point, E was being supplemented with formula milk."
"In respect of the CD from Great Ormond Street Hospital, skeletal survey dated11 October 2012 , seven months, 25 days' old, 24 images of technically-adequate quality. No abnormality in the heart, lungs or abdominal bowel gas pattern. There is mild deformity of the right distal humerus in keeping with a previous fracture. The long bones of the lower limbs appear subjectively slightly osteopenic, but no local pathology is evident."
"Question 1: The bone density which has reported at GOSH by several professionals now: any reason why the bone density was not seen on the Northampton x-rays as E's vitamin D deficiency and serum calcium levels was a lot lower as they introduced supplements after these had been done. Answer: The possibilities here are (a) it was not present; (b) it was present, but not visible on the Northampton radiographs; or (c) there were technical differences in the radiographic acquisition in the two hospitals that would account for the differences. Radiographs are poor at assessing bone density in young children. "
"E herself has not sustained any fractures since those detected in infancy. Fracture susceptibility in the mildest form of osteogenesis imperfecta, namely type 1, usually manifests when infants become toddlers, and fall over. On the occasion when E fell frequently prior to having her glasses, she did not fracture any bones. A previous assessment through clinical genetics led to a genetic testing of two genes most commonly associated with OI type 1, namely COL1A1 and COL1A2. The results shared with me in the case bundle show no mutations were found, although there was note made that larger changes within these genes, accounting for 2 per cent for those with OI, might not have been detected through this test. There were no grounds indicating a clinical need to pursue further testing. "