Jones v. Principi

16 Vet. App. 219, 2002 U.S. Vet. App. LEXIS 579, 2002 WL 1808588
CourtUnited States Court of Appeals for Veterans Claims
DecidedAugust 7, 2002
Docket00-669
StatusPublished
Cited by5 cases

This text of 16 Vet. App. 219 (Jones v. Principi) is published on Counsel Stack Legal Research, covering United States Court of Appeals for Veterans Claims primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Jones v. Principi, 16 Vet. App. 219, 2002 U.S. Vet. App. LEXIS 579, 2002 WL 1808588 (Cal. 2002).

Opinion

STEINBERG, Judge.

The appellant, the daughter of a Vietnam veteran, appeals through counsel a March 15, 2000, decision of the Board of Veterans’ Appeals (Board or BVA) that denied entitlement to her, as a child of a Vietnam veteran, for a Department of Veterans Affairs (VA) monetary allowance for a disability resulting from spina bifida. Record (R.) at 6. The appellant filed a brief and a reply brief, and the Secretary filed a brief. Oral argument was held on April 23, 2002. On April 25, 2002, the Court ordered supplemental briefing from the parties. In response to the Court’s order, the Secretary filed a supplemental record on appeal (ROA) and a supplemental memorandum of law, and the appellant filed a reply to the Secretary’s supplemental memorandum. The Court has jurisdiction over the case under 38 U.S.C. §§ 7252(a) and 7266(a). For the reasons set forth below, the Court will vacate the Board decision on appeal and remand the matter for readjudication.

I. Relevant Background

The veteran served in the U.S. Navy from July 1965 to November 1968 and from December 1968 to July 1971. R. at 9, 130. He had service in Vietnam and received the National Defense Service Medal with Bronze Star, the Vietnam Service Medal, and three Purple Heart Medals. R. at 9. The appellant was born on June 6,1986. R. at 133.

A December 1997 medical report from Dr. MacDonald, a private physician, recorded that the appellant was an “11-year-old girl [who] is seen for neurological follow-up of her encephaloeele”, and stated that he “would like to ... repeat her MRI [ (Magnetic Resonance Imaging) ] scan of the posterior fossa of the brain and cervical spine area since she did have a syrinx in the past and we should follow that and *221 see if there is any major change.” R. at 145. (Encephaloeele is “hernia of part of the brain and meninges through a skull defect.” Dorland’s Illustrated Medioal DiCtionaey 548 (28th ed.1994) [hereinafter Dorland’s]. Meninges are “the three membranes that envelop the brain and spinal cord”. Dorland’s at 1010. A syrinx is “a tube or pipe ... [or] a fistula ... [or] an abnormal cavity in the spinal cord in syringomyelia.” DoRland’s at 1647.)

In January 1998, the veteran filed an application for spina bifida benefits for his daughter. R. at 137. In a note attached to the application, the veteran stated:

My daughter, Michelle Colleen Jones, was born on 6-6-86 at St. Joseph’s Hospital, Denver[,] Colorado. Three & 1/2 weeks prior to [b]irth, it was detected on ultrasound that the child would have an occipital encephaloeele [hereinafter OE], a spinal cord defect, called a [n]eural tube defect.
Along with this, she has hydrocephalus, controlled by bilateral shunts, and [is] also [d]iagnosed with a Chiari II [mjalformation.
Her initial physician Dr. Peter Hu-lac[,] a [n]eo-[n]atologist[,] ... and also Dr. Larry McLenny[, a] pediatric neuro-surgeonf,] informed my wife [and me] that this is in the [s]pina [b]ifida family in the superior part of the spine.

R. at 138. (OE is “an encephaloeele in the occipital region”. Dorland’s at 549. Occipital means “located near the occipital bone, as the occipital lobe of the brain”. Dorland’s at 1167.) A February 1998 letter from Dr. MeLellan, a private physician, described the appellant as “an 11-year-old girl with an encephaloeele” and notes that “[t]his is associated with hydrocephalus” and that “[o]ther anatomic anomalies coexistent with the encephaloeele include a Chiari [m]alformation which involves a herniation of a portion of cerebellum through the skull outlet[; s]he [also] has a syrinx in the cervical cord”. R. at 157.

In March 1998, a VA regional office (RO) denied the appellant’s claim. R. at 162. The RO stated that “[e]urrent regulations allow a grant of benefits only where there is protrusion of the meninges through the vertebrae or bony encasement” (R. at 161) (the Court can find no VA regulation with such a limitation, and the Secretary was unable to provide any basis for the RO statement (Supplemental memorandum at 2-3)), and the RO concluded that “[b]y definitionf,] an encephal-ocele, which is the condition that Michelle is diagnosed with, is not spina bifida” (R. at 162). A Notice of Disagreement was filed on behalf of the appellant (R. at 165), and the RO issued a Statement of the Case (R. at 174-78).

An April 1998 letter from Dr. Steidler, a private neuroradiologist, stated:

This letter is in regards to Michelle C. Jones’ diagnoses of encephaloeele, Chi-ari II malformation, and cervical syrinx as it relates to spina bifida. Neural tube defects include multiple abnormalities, only one of which is spina bifida. Spina bifida can be very mild and incidental on radiographs, often at the lumbar region, and of no clinical significance. However, multiple other neural tube closure defects at other levels of the spine as well as the brain and skull can be seen with multiple known associated anomalies such as Chiari II malformation, syrin-gohyrdromyelia, hyrdoeephalus, callosal dysgenesis, etc. Therefore, the neural tube closure defects, with spina bifida referring to a finding which is often at the less serious end of this spectrum[,] are considered to be a spectrum of related abnormalities.

R. at 186. A May 1998 letter from Dr. Houston, also a private neuroradiologist, stated: “[OE] is a defect in the skull and *222 dura with extracranial extension of the intracranial structures located in the occipital region. One etiology for cephalocele is failure of closure of the sites of primary neural tube closure.” R. at 187. In a May 1998 letter, Dr. MacDonald stated: “[The appellant] had the [OE] with secondary neurologic chronic problems including the shunt, truncal instability, esotrophia, and spinal cord cyst. I think they have to realize that this is a neural tube defect and that an [OE] is a form of spina bifida or open spine”. R. at 189. A May 1998 letter from Dr. Yock, a private physician, stated that “it is medically reasonable to consider [OE] in the same category as ‘spina bifida’ from both emryologic and clinical perspectives.” R. at 191.

In July 1998, the VARO requested an advisory opinion from the VA Director of Compensation and Pension Service. R. at 193-94. This request was then relayed to the VA Under Secretary for Health. R. at 196. In response, Dr. Mather, VA Chief Public Health and Environmental Hazards Officer, stated in pertinent part:

[The appellant] was born with an [OE] associated with hydrocephalus and Arnold-Chiari malformation. She also has a spinal cord syrinx. The eneephaloco-cele is definitely a neural tube defect, not by embryology or sequelae. In Veterans and Agent Orange: Update 1996, the National Academy of Sciences cited four veterans studies as the reason for their conclusion that limited or suggestive evidence of an association between agent orange and the birth defect, spina bifida, existed. Two of the four veterans studies (the Ranch Hand and the Australian veterans studies) refer specifically to neural tube defects and not to spina bifida per se.

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Cite This Page — Counsel Stack

Bluebook (online)
16 Vet. App. 219, 2002 U.S. Vet. App. LEXIS 579, 2002 WL 1808588, Counsel Stack Legal Research, https://law.counselstack.com/opinion/jones-v-principi-cavc-2002.